Short description of cell lines. Species: human (line names begin with I)

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For information, get in touch with: Dott.ssa Paola Visconti
Email: paola.visconti@hsanmartino.it

P. Romano, A. Manniello et al. Nucl Acids Res 2009 37:D925-D932.
DOI: doi:10.1093/nar/gkn730; PMID: 18927105

Short description of cell lines
Species: human (all ethnic groups)

- By clicking on the cell line name, you will retrieve the detailed description of the cell line
- By clicking on one of the terms between parentheses, you will retrieve the list of all relevant cell line

1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

I-B92 (amnion, trisomy 21 / Down syndrome) - GGB
I-P94 (amnion, trisomy 21 / Down syndrome) - GGB
I1094 (fibroblast) - GGB
I1686 (fibroblast) - GGB
I2586 (fibroblast, achondrogenesis I) - GGB
IC86 (lymphocyte, trisomy 21 / Down syndrome) - GGB
IG88IL2 (lymphocyte) - GGB
IG88ls (lymphocyte) - GGB
IGA001/83 (amnion) - GEIMM
IGA001/85 (amnion, propionicacidemia I) - GEIMM
IGA001/92 (amnion, maple syrup urine disease) - GEIMM
IGA001/99 (amnion, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGA004/90 (amnion, glycogen storage disease II) - GEIMM
IGA004/95 (amnion, Krabbe disease) - GEIMM
IGA004/99 (amnion, methylmalonicacidemia) - GEIMM
IGA005/84 (amnion, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA005/98 (amnion, methylmalonicacidemia) - GEIMM
IGA007/96 (amnion, mucolipidosis II) - GEIMM
IGA008/82 (amnion, glycogen storage disease II) - GEIMM
IGA009/84 (amnion, Niemann-Pick disease, type A) - GEIMM
IGA009/98 (amnion, mucolipidosis II) - GEIMM
IGA010/89 (amnion, Niemann-Pick disease, type A) - GEIMM
IGA013/83 (amnion, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA015/96 (amnion, galactosemia) - GEIMM
IGA016/84 (amnion, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGA017/99 (amnion, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA018/85 (amnion, Tay-Sachs disease) - GEIMM
IGA020/90 (amnion, metachromatic leukodystrophy, late-infantile) - GEIMM
IGA022/82 (amnion, fucosidosis) - GEIMM
IGA022/99 (amnion, Menkes syndrome) - GEIMM
IGA024/90 (amnion, Niemann-Pick disease, type A) - GEIMM
IGA028/83 (amnion, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA031/82 (amnion, glycogen storage disease II) - GEIMM
IGA031/87 (amnion) - GEIMM
IGA033/83 (amnion, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA036/83 (amnion, glycogen storage disease II) - GEIMM
IGA040/78 (amnion, fucosidosis) - GEIMM
IGA040/82 (amnion, propionicacidemia I) - GEIMM
IGA058/80 (amnion, glycogen storage disease II) - GEIMM
IGA063/80 (amnion, mucopolysaccharidosis type VI) - GEIMM
IGA188/78 (amnion, mannosidosis, alpha b, lysosomal) - GEIMM
IGF001/00 (skin, fibroblast) - GEIMM
IGF001/01 (skin, fibroblast) - GEIMM
IGF001/77 (skin, fibroblast) - GEIMM
IGF001/78 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF001/80 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF001/81 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF001/83 (skin, fibroblast) - GEIMM
IGF001/84 (skin, fibroblast) - GEIMM
IGF001/85 (skin, fibroblast) - GEIMM
IGF001/86 (skin, fibroblast) - GEIMM
IGF001/87 (skin, fibroblast) - GEIMM
IGF001/90 (skin, fibroblast, Steinert disease) - GEIMM
IGF001/91 (skin, fibroblast, Charcot-Marie-Tooth disease) - GEIMM
IGF001/93 (skin, fibroblast) - GEIMM
IGF001/94 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF001/95 (skin, fibroblast) - GEIMM
IGF001/96 (skin, fibroblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF001/97 (skin, fibroblast) - GEIMM
IGF001/98 (skin, fibroblast, Glutaricacidemia I) - GEIMM
IGF001/99 (skin, fibroblast) - GEIMM
IGF002/00 (skin, fibroblast, Krabbe disease) - GEIMM
IGF002/01 (skin, fibroblast) - GEIMM
IGF002/77 (skin, fibroblast) - GEIMM
IGF002/78 (skin, fibroblast, phenylketonuria II) - GEIMM
IGF002/79 (skin, fibroblast) - GEIMM
IGF002/80 (skin, fibroblast, Fanconi-Bickel syndrome) - GEIMM
IGF002/81 (skin, fibroblast) - GEIMM
IGF002/82 (skin, fibroblast) - GEIMM
IGF002/83 (skin, fibroblast) - GEIMM
IGF002/85 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF002/86 (skin, fibroblast) - GEIMM
IGF002/87 (skin, fibroblast) - GEIMM
IGF002/88 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF002/90 (skin, fibroblast) - GEIMM
IGF002/91 (skin, fibroblast) - GEIMM
IGF002/92 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF002/93 (skin, fibroblast) - GEIMM
IGF002/94 (skin, fibroblast) - GEIMM
IGF002/95 (skin, fibroblast, McCune-Albright sindrome) - GEIMM
IGF002/96 (skin, fibroblast, DiGeorge syndrome) - GEIMM
IGF002/97 (skin, fibroblast) - GEIMM
IGF002/98 (skin, fibroblast) - GEIMM
IGF002/99 (skin, fibroblast) - GEIMM
IGF003/00 (skin, fibroblast) - GEIMM
IGF003/01 (skin, fibroblast) - GEIMM
IGF003/77 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF003/80 (skin, fibroblast) - GEIMM
IGF003/81 (skin, fibroblast) - GEIMM
IGF003/82 (skin, fibroblast, metatropic dwarfism, type II) - GEIMM
IGF003/83 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF003/85 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF003/86 (skin, fibroblast) - GEIMM
IGF003/87 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF003/88 (skin, fibroblast) - GEIMM
IGF003/89 (skin, fibroblast, Freeman-Sheldon syndrome) - GEIMM
IGF003/92 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF003/93 (skin, fibroblast) - GEIMM
IGF003/94 (skin, fibroblast) - GEIMM
IGF003/96 (skin, fibroblast) - GEIMM
IGF003/97 (skin, fibroblast) - GEIMM
IGF003/98 (skin, fibroblast) - GEIMM
IGF003/99 (skin, fibroblast) - GEIMM
IGF004/00 (skin, fibroblast, salla disease) - GEIMM
IGF004/01 (skin, fibroblast) - GEIMM
IGF004/78 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF004/79 (skin, fibroblast) - GEIMM
IGF004/81 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF004/82 (skin, fibroblast) - GEIMM
IGF004/83 (skin, fibroblast) - GEIMM
IGF004/84 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF004/85 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF004/86 (skin, fibroblast) - GEIMM
IGF004/87 (skin, fibroblast) - GEIMM
IGF004/89 (skin, fibroblast, metatropic dwarfism, type II) - GEIMM
IGF004/91 (skin, fibroblast, Ehlers-Danlos syndrome, type IV, autosomal dominant) - GEIMM
IGF004/93 (skin, fibroblast) - GEIMM
IGF004/94 (skin, fibroblast) - GEIMM
IGF004/96 (skin, fibroblast, Cockayne syndrome) - GEIMM
IGF004/97 (skin, fibroblast) - GEIMM
IGF004/98 (skin, fibroblast, neuropathy, giant axonal) - GEIMM
IGF004/99 (skin, fibroblast) - GEIMM
IGF005/00 (skin, fibroblast) - GEIMM
IGF005/01 (skin, fibroblast) - GEIMM
IGF005/77 (skin, fibroblast) - GEIMM
IGF005/80 (skin, fibroblast) - GEIMM
IGF005/82 (skin, fibroblast) - GEIMM
IGF005/83 (skin, fibroblast) - GEIMM
IGF005/84 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF005/85 (skin, fibroblast) - GEIMM
IGF005/86 (skin, fibroblast) - GEIMM
IGF005/87 (skin, fibroblast) - GEIMM
IGF005/89 (skin, fibroblast) - GEIMM
IGF005/91 (skin, fibroblast) - GEIMM
IGF005/92 (skin, fibroblast, NARP mutation) - GEIMM
IGF005/93 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF005/94 (skin, fibroblast) - GEIMM
IGF005/95 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF005/96 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF005/97 (skin, fibroblast) - GEIMM
IGF005/98 (skin, fibroblast, glycogen storage disease IV) - GEIMM
IGF005/99 (skin, fibroblast) - GEIMM
IGF006/00 (skin, fibroblast) - GEIMM
IGF006/01 (skin, fibroblast) - GEIMM
IGF006/77 (skin, fibroblast) - GEIMM
IGF006/79 (skin, fibroblast) - GEIMM
IGF006/80 (skin, fibroblast, camptomelic dwarfism) - GEIMM
IGF006/81 (skin, fibroblast) - GEIMM
IGF006/82 (skin, fibroblast, hypophosphatasia infantile) - GEIMM
IGF006/83 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF006/84 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF006/85 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF006/86 (skin, fibroblast) - GEIMM
IGF006/87 (skin, fibroblast) - GEIMM
IGF006/89 (skin, fibroblast) - GEIMM
IGF006/91 (skin, fibroblast) - GEIMM
IGF006/92 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF006/93 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF006/94 (skin, fibroblast, neuraminidase deficiency with beta-galactosidase deficiency) - GEIMM
IGF006/95 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF006/96 (skin, fibroblast) - GEIMM
IGF006/97 (skin, fibroblast) - GEIMM
IGF006/98 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF006/99 (skin, fibroblast) - GEIMM
IGF007/00 (skin, fibroblast) - GEIMM
IGF007/01 (skin, fibroblast) - GEIMM
IGF007/79 (skin, fibroblast) - GEIMM
IGF007/80 (skin, fibroblast) - GEIMM
IGF007/81 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF007/84 (skin, fibroblast) - GEIMM
IGF007/85 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF007/86 (skin, fibroblast) - GEIMM
IGF007/87 (skin, fibroblast) - GEIMM
IGF007/89 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF007/90 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF007/91 (skin, fibroblast) - GEIMM
IGF007/92 (skin, fibroblast, Cockayne syndrome) - GEIMM
IGF007/93 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF007/95 (skin, fibroblast) - GEIMM
IGF007/96 (skin, fibroblast) - GEIMM
IGF007/97 (skin, fibroblast) - GEIMM
IGF007/98 (skin, fibroblast, Davidson disease) - GEIMM
IGF007/99 (skin, fibroblast) - GEIMM
IGF008/00 (skin, fibroblast) - GEIMM
IGF008/01 (skin, fibroblast) - GEIMM
IGF008/78 (skin, fibroblast) - GEIMM
IGF008/79 (skin, fibroblast) - GEIMM
IGF008/80 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF008/81 (skin, fibroblast) - GEIMM
IGF008/82 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF008/84 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF008/86 (skin, fibroblast) - GEIMM
IGF008/87 (skin, fibroblast) - GEIMM
IGF008/88 (skin, fibroblast) - GEIMM
IGF008/89 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF008/92 (skin, fibroblast) - GEIMM
IGF008/94 (skin, fibroblast) - GEIMM
IGF008/96 (skin, fibroblast) - GEIMM
IGF008/97 (skin, fibroblast) - GEIMM
IGF008/98 (skin, fibroblast) - GEIMM
IGF008/99 (skin, fibroblast) - GEIMM
IGF009/00 (skin, fibroblast) - GEIMM
IGF009/01 (skin, fibroblast) - GEIMM
IGF009/77 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF009/78 (skin, fibroblast) - GEIMM
IGF009/80 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF009/81 (skin, fibroblast, neuronal ceroid-lipofuscinosis infantile Finnish type) - GEIMM
IGF009/82 (skin, fibroblast) - GEIMM
IGF009/84 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF009/85 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF009/86 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF009/87 (skin, fibroblast) - GEIMM
IGF009/88 (skin, fibroblast) - GEIMM
IGF009/89 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF009/90 (skin, fibroblast, Zellweger syndrome) - GEIMM
IGF009/91 (skin, fibroblast) - GEIMM
IGF009/92 (skin, fibroblast) - GEIMM
IGF009/93 (skin, fibroblast, Krabbe disease) - GEIMM
IGF009/94 (skin, fibroblast) - GEIMM
IGF009/96 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF009/97 (skin, fibroblast) - GEIMM
IGF009/98 (skin, fibroblast, Pallister Killian syndrome) - GEIMM
IGF009/99 (skin, fibroblast) - GEIMM
IGF010/00 (skin, fibroblast) - GEIMM
IGF010/77 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF010/78 (skin, fibroblast) - GEIMM
IGF010/80 (skin, fibroblast) - GEIMM
IGF010/81 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF010/83 (skin, fibroblast) - GEIMM
IGF010/84 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF010/85 (skin, fibroblast) - GEIMM
IGF010/86 (skin, fibroblast) - GEIMM
IGF010/87 (skin, fibroblast) - GEIMM
IGF010/88 (skin, fibroblast) - GEIMM
IGF010/89 (skin, fibroblast) - GEIMM
IGF010/90 (skin, fibroblast, Wilson disease) - GEIMM
IGF010/91 (skin, fibroblast) - GEIMM
IGF010/92 (skin, fibroblast) - GEIMM
IGF010/93 (skin, fibroblast) - GEIMM
IGF010/94 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF010/96 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF010/97 (skin, fibroblast) - GEIMM
IGF010/98 (skin, fibroblast) - GEIMM
IGF010/99 (skin, fibroblast) - GEIMM
IGF011/00 (skin, fibroblast) - GEIMM
IGF011/01 (skin, fibroblast) - GEIMM
IGF011/77 (skin, fibroblast, Ehlers-Danlos syndrome, type I) - GEIMM
IGF011/78 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF011/80 (skin, fibroblast) - GEIMM
IGF011/81 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF011/82 (skin, fibroblast, amaurotic family idiocy, juvenile type/neuronal ceroid lipofuscinosis) - GEIMM
IGF011/83 (skin, fibroblast) - GEIMM
IGF011/84 (skin, fibroblast) - GEIMM
IGF011/85 (skin, fibroblast) - GEIMM
IGF011/86 (skin, fibroblast) - GEIMM
IGF011/87 (skin, fibroblast) - GEIMM
IGF011/89 (skin, fibroblast) - GEIMM
IGF011/90 (skin, fibroblast) - GEIMM
IGF011/91 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF011/92 (skin, fibroblast, Ehlers-Danlos syndrome, type I) - GEIMM
IGF011/93 (skin, fibroblast) - GEIMM
IGF011/94 (skin, fibroblast) - GEIMM
IGF011/96 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF011/97 (skin, fibroblast) - GEIMM
IGF011/98 (skin, fibroblast) - GEIMM
IGF011/99 (skin, fibroblast, osteopetrosis autosomal recessive) - GEIMM
IGF012/00 (skin, fibroblast) - GEIMM
IGF012/01 (skin, fibroblast) - GEIMM
IGF012/77 (skin, fibroblast) - GEIMM
IGF012/78 (skin, fibroblast) - GEIMM
IGF012/80 (skin, fibroblast) - GEIMM
IGF012/81 (skin, fibroblast, tyrosine transaminase deficiency) - GEIMM
IGF012/82 (skin, fibroblast) - GEIMM
IGF012/83 (skin, fibroblast) - GEIMM
IGF012/84 (skin, fibroblast) - GEIMM
IGF012/85 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF012/86 (skin, fibroblast) - GEIMM
IGF012/87 (skin, fibroblast, spondyloepiphyseal dysplasia, congenital) - GEIMM
IGF012/89 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF012/90 (skin, fibroblast, hydrocephalus, agyria, retinal dysplasia Hard syndrome/Walker-Warburg) - GEIMM
IGF012/91 (skin, fibroblast, Krabbe disease) - GEIMM
IGF012/92 (skin, fibroblast) - GEIMM
IGF012/93 (skin, fibroblast) - GEIMM
IGF012/94 (skin, fibroblast) - GEIMM
IGF012/96 (skin, fibroblast) - GEIMM
IGF012/98 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF012/99 (skin, fibroblast, Austin) - GEIMM
IGF013/00 (skin, fibroblast) - GEIMM
IGF013/01 (skin, fibroblast) - GEIMM
IGF013/77 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF013/78 (skin, fibroblast) - GEIMM
IGF013/80 (skin, fibroblast) - GEIMM
IGF013/81 (skin, fibroblast, tyrosine transaminase deficiency) - GEIMM
IGF013/82 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF013/84 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF013/85 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF013/86 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF013/87 (skin, fibroblast) - GEIMM
IGF013/89 (skin, fibroblast) - GEIMM
IGF013/90 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF013/91 (skin, fibroblast) - GEIMM
IGF013/92 (skin, fibroblast) - GEIMM
IGF013/93 (skin, fibroblast) - GEIMM
IGF013/94 (skin, fibroblast) - GEIMM
IGF013/95 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF013/96 (skin, fibroblast) - GEIMM
IGF013/99 (skin, fibroblast, sulfatidosis, juvenile, Austin type) - GEIMM
IGF014/00 (skin, fibroblast) - GEIMM
IGF014/01 (skin, fibroblast) - GEIMM
IGF014/78 (skin, fibroblast) - GEIMM
IGF014/80 (skin, fibroblast) - GEIMM
IGF014/81 (skin, fibroblast) - GEIMM
IGF014/82 (skin, fibroblast) - GEIMM
IGF014/83 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF014/84 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF014/85 (skin, fibroblast) - GEIMM
IGF014/86 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF014/87 (skin, fibroblast) - GEIMM
IGF014/89 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF014/90 (skin, fibroblast, osteoporosis-pseudoglioma syndrome) - GEIMM
IGF014/91 (skin, fibroblast, Lesch-Nyhan syndrome) - GEIMM
IGF014/92 (skin, fibroblast) - GEIMM
IGF014/93 (skin, fibroblast) - GEIMM
IGF014/94 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF014/95 (skin, fibroblast) - GEIMM
IGF014/96 (skin, fibroblast) - GEIMM
IGF014/97 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF014/98 (skin, fibroblast) - GEIMM
IGF014/99 (skin, fibroblast) - GEIMM
IGF015/00 (skin, fibroblast) - GEIMM
IGF015/01 (skin, fibroblast) - GEIMM
IGF015/78 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF015/80 (skin, fibroblast) - GEIMM
IGF015/82 (skin, fibroblast) - GEIMM
IGF015/83 (skin, fibroblast) - GEIMM
IGF015/84 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF015/85 (skin, fibroblast) - GEIMM
IGF015/86 (skin, fibroblast) - GEIMM
IGF015/87 (skin, fibroblast) - GEIMM
IGF015/90 (skin, fibroblast, osteoporosis-pseudoglioma syndrome) - GEIMM
IGF015/91 (skin, fibroblast) - GEIMM
IGF015/94 (skin, fibroblast) - GEIMM
IGF015/95 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF015/96 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF015/97 (skin, fibroblast, def. PDH complex thiamine responsive) - GEIMM
IGF015/98 (skin, fibroblast) - GEIMM
IGF015/99 (skin, fibroblast) - GEIMM
IGF016/00 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF016/01 (skin, fibroblast) - GEIMM
IGF016/77 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF016/78 (skin, fibroblast, Ehlers-Danlos syndrome) - GEIMM
IGF016/80 (skin, fibroblast) - GEIMM
IGF016/81 (skin, fibroblast) - GEIMM
IGF016/82 (skin, fibroblast, tyrosine transaminase deficiency) - GEIMM
IGF016/83 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF016/84 (skin, fibroblast) - GEIMM
IGF016/85 (skin, fibroblast) - GEIMM
IGF016/86 (skin, fibroblast, Marinesco-Sjogren syndrome) - GEIMM
IGF016/87 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF016/89 (skin, fibroblast) - GEIMM
IGF016/90 (skin, fibroblast) - GEIMM
IGF016/91 (skin, fibroblast) - GEIMM
IGF016/92 (skin, fibroblast) - GEIMM
IGF016/93 (skin, fibroblast) - GEIMM
IGF016/94 (skin, fibroblast) - GEIMM
IGF016/95 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF016/96 (skin, fibroblast, Krabbe disease) - GEIMM
IGF016/97 (skin, fibroblast) - GEIMM
IGF016/98 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF016/99 (skin, fibroblast) - GEIMM
IGF017/00 (skin, fibroblast, mucopolysaccharidosis type III D) - GEIMM
IGF017/01 (skin, fibroblast) - GEIMM
IGF017/76 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF017/78 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF017/80 (skin, fibroblast) - GEIMM
IGF017/82 (skin, fibroblast, tyrosine transaminase deficiency) - GEIMM
IGF017/83 (skin, fibroblast) - GEIMM
IGF017/84 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF017/85 (skin, fibroblast) - GEIMM
IGF017/86 (skin, fibroblast) - GEIMM
IGF017/87 (skin, fibroblast) - GEIMM
IGF017/89 (skin, fibroblast) - GEIMM
IGF017/90 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF017/91 (skin, fibroblast) - GEIMM
IGF017/92 (skin, fibroblast, Costello syndrome) - GEIMM
IGF017/93 (skin, fibroblast) - GEIMM
IGF017/95 (skin, fibroblast, leukoencephalopathy with vanishing white matter) - GEIMM
IGF017/96 (skin, fibroblast) - GEIMM
IGF017/97 (skin, fibroblast) - GEIMM
IGF017/98 (skin, fibroblast) - GEIMM
IGF017/99 (skin, fibroblast) - GEIMM
IGF018/00 (skin, fibroblast, X duplication) - GEIMM
IGF018/01 (skin, fibroblast) - GEIMM
IGF018/77 (skin, fibroblast, mucopolysaccharidosis type III D) - GEIMM
IGF018/78 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF018/80 (skin, fibroblast) - GEIMM
IGF018/81 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF018/82 (skin, fibroblast) - GEIMM
IGF018/83 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF018/84 (skin, fibroblast) - GEIMM
IGF018/85 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF018/86 (skin, fibroblast) - GEIMM
IGF018/87 (skin, fibroblast) - GEIMM
IGF018/88 (skin, fibroblast) - GEIMM
IGF018/89 (skin, fibroblast) - GEIMM
IGF018/90 (skin, fibroblast, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF018/91 (skin, fibroblast) - GEIMM
IGF018/92 (skin, fibroblast) - GEIMM
IGF018/93 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF018/94 (skin, fibroblast, Krabbe disease) - GEIMM
IGF018/95 (skin, fibroblast) - GEIMM
IGF018/96 (skin, fibroblast) - GEIMM
IGF018/97 (skin, fibroblast) - GEIMM
IGF018/98 (skin, fibroblast) - GEIMM
IGF018/99 (skin, fibroblast) - GEIMM
IGF019/00 (skin, fibroblast) - GEIMM
IGF019/01 (skin, fibroblast) - GEIMM
IGF019/77 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF019/78 (skin, fibroblast) - GEIMM
IGF019/80 (skin, fibroblast, neuroaxonal dystrophy, infantile) - GEIMM
IGF019/82 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF019/84 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF019/85 (skin, fibroblast) - GEIMM
IGF019/86 (skin, fibroblast) - GEIMM
IGF019/87 (skin, fibroblast, ataxia telangiectasia) - GEIMM
IGF019/88 (skin, fibroblast) - GEIMM
IGF019/89 (skin, fibroblast) - GEIMM
IGF019/90 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF019/91 (skin, fibroblast) - GEIMM
IGF019/92 (skin, fibroblast) - GEIMM
IGF019/93 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF019/96 (skin, fibroblast, acyl-CoA dehydrogenase, long-chain, deficiency) - GEIMM
IGF019/97 (skin, fibroblast) - GEIMM
IGF019/98 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF019/99 (skin, fibroblast) - GEIMM
IGF020/00 (skin, fibroblast, SURF1) - GEIMM
IGF020/01 (skin, fibroblast) - GEIMM
IGF020/78 (skin, fibroblast) - GEIMM
IGF020/80 (skin, fibroblast) - GEIMM
IGF020/82 (skin, fibroblast) - GEIMM
IGF020/83 (skin, fibroblast, multiple carboxylase deficiency, late-onset) - GEIMM
IGF020/84 (skin, fibroblast, Krabbe disease) - GEIMM
IGF020/85 (skin, fibroblast) - GEIMM
IGF020/86 (skin, fibroblast) - GEIMM
IGF020/87 (skin, fibroblast) - GEIMM
IGF020/88 (skin, fibroblast) - GEIMM
IGF020/89 (skin, fibroblast) - GEIMM
IGF020/90 (skin, fibroblast) - GEIMM
IGF020/91 (skin, fibroblast) - GEIMM
IGF020/92 (skin, fibroblast) - GEIMM
IGF020/93 (skin, fibroblast, Krabbe disease) - GEIMM
IGF020/94 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF020/95 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF020/96 (skin, fibroblast, proteolipid protein, myelin) - GEIMM
IGF020/97 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF020/98 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF020/99 (skin, fibroblast) - GEIMM
IGF021/00 (skin, fibroblast) - GEIMM
IGF021/01 (skin, fibroblast) - GEIMM
IGF021/78 (skin, fibroblast) - GEIMM
IGF021/82 (skin, fibroblast) - GEIMM
IGF021/83 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF021/84 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF021/85 (skin, fibroblast) - GEIMM
IGF021/86 (skin, fibroblast, Kartagener syndrome X) - GEIMM
IGF021/87 (skin, fibroblast, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF021/88 (skin, fibroblast) - GEIMM
IGF021/90 (skin, fibroblast) - GEIMM
IGF021/91 (skin, fibroblast) - GEIMM
IGF021/92 (skin, fibroblast) - GEIMM
IGF021/93 (skin, fibroblast) - GEIMM
IGF021/94 (skin, fibroblast, fructose-1, 6-diphosphatase deficiency) - GEIMM
IGF021/95 (skin, fibroblast) - GEIMM
IGF021/96 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF021/97 (skin, fibroblast) - GEIMM
IGF021/98 (skin, fibroblast) - GEIMM
IGF021/99 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF022/00 (skin, fibroblast) - GEIMM
IGF022/01 (skin, fibroblast) - GEIMM
IGF022/77 (skin, fibroblast) - GEIMM
IGF022/78 (skin, fibroblast) - GEIMM
IGF022/79 (skin, fibroblast) - GEIMM
IGF022/80 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF022/81 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF022/82 (skin, fibroblast) - GEIMM
IGF022/83 (skin, fibroblast) - GEIMM
IGF022/84 (skin, fibroblast) - GEIMM
IGF022/85 (skin, fibroblast) - GEIMM
IGF022/86 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF022/87 (skin, fibroblast, Lesch-Nyhan syndrome) - GEIMM
IGF022/88 (skin, fibroblast) - GEIMM
IGF022/89 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF022/90 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF022/91 (skin, fibroblast) - GEIMM
IGF022/92 (skin, fibroblast) - GEIMM
IGF022/93 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF022/94 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF022/95 (skin, fibroblast) - GEIMM
IGF022/96 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF022/97 (skin, fibroblast) - GEIMM
IGF022/98 (skin, fibroblast) - GEIMM
IGF022/99 (skin, fibroblast) - GEIMM
IGF023/00 (skin, fibroblast) - GEIMM
IGF023/01 (skin, fibroblast) - GEIMM
IGF023/77 (skin, fibroblast) - GEIMM
IGF023/78 (skin, fibroblast) - GEIMM
IGF023/79 (skin, fibroblast) - GEIMM
IGF023/81 (skin, fibroblast) - GEIMM
IGF023/83 (skin, fibroblast, Fanconi-Bickel syndrome) - GEIMM
IGF023/84 (skin, fibroblast, Engelmann disease) - GEIMM
IGF023/85 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF023/86 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF023/87 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF023/88 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF023/90 (skin, fibroblast) - GEIMM
IGF023/91 (skin, fibroblast) - GEIMM
IGF023/93 (skin, fibroblast) - GEIMM
IGF023/94 (skin, fibroblast) - GEIMM
IGF023/95 (skin, fibroblast) - GEIMM
IGF023/96 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF023/97 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF023/98 (skin, fibroblast) - GEIMM
IGF023/99 (skin, fibroblast) - GEIMM
IGF024/00 (skin, fibroblast, citrullinemia) - GEIMM
IGF024/01 (skin, fibroblast) - GEIMM
IGF024/77 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF024/78 (skin, fibroblast) - GEIMM
IGF024/79 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF024/81 (skin, fibroblast, dibasicaminoaciduria II) - GEIMM
IGF024/82 (skin, fibroblast) - GEIMM
IGF024/83 (skin, fibroblast) - GEIMM
IGF024/85 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF024/86 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF024/88 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF024/90 (skin, fibroblast) - GEIMM
IGF024/91 (skin, fibroblast) - GEIMM
IGF024/92 (skin, fibroblast) - GEIMM
IGF024/93 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF024/94 (skin, fibroblast) - GEIMM
IGF024/95 (skin, fibroblast) - GEIMM
IGF024/96 (skin, fibroblast) - GEIMM
IGF024/97 (skin, fibroblast) - GEIMM
IGF024/98 (skin, fibroblast) - GEIMM
IGF024/99 (skin, fibroblast) - GEIMM
IGF025/00 (skin, fibroblast) - GEIMM
IGF025/01 (skin, fibroblast) - GEIMM
IGF025/77 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF025/78 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF025/80 (skin, fibroblast) - GEIMM
IGF025/81 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF025/82 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF025/83 (skin, fibroblast) - GEIMM
IGF025/84 (skin, fibroblast) - GEIMM
IGF025/85 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF025/86 (skin, fibroblast) - GEIMM
IGF025/87 (skin, fibroblast) - GEIMM
IGF025/88 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF025/89 (skin, fibroblast, Krabbe disease) - GEIMM
IGF025/90 (skin, fibroblast) - GEIMM
IGF025/91 (skin, fibroblast, acyl-CoA dehydrogenase, long-chain, deficiency) - GEIMM
IGF025/92 (skin, fibroblast, arthrogryposis multiplex congenita) - GEIMM
IGF025/93 (skin, fibroblast) - GEIMM
IGF025/95 (skin, fibroblast, fucosidosis) - GEIMM
IGF025/96 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF025/97 (skin, fibroblast) - GEIMM
IGF025/98 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF025/99 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF026/00 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF026/01 (skin, fibroblast) - GEIMM
IGF026/77 (skin, fibroblast) - GEIMM
IGF026/78 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF026/80 (skin, fibroblast) - GEIMM
IGF026/82 (skin, fibroblast) - GEIMM
IGF026/83 (skin, fibroblast) - GEIMM
IGF026/84 (skin, fibroblast) - GEIMM
IGF026/85 (skin, fibroblast) - GEIMM
IGF026/86 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF026/87 (skin, fibroblast) - GEIMM
IGF026/88 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF026/89 (skin, fibroblast) - GEIMM
IGF026/90 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF026/91 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF026/92 (skin, fibroblast) - GEIMM
IGF026/93 (skin, fibroblast) - GEIMM
IGF026/95 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF026/96 (skin, fibroblast) - GEIMM
IGF026/97 (skin, fibroblast) - GEIMM
IGF026/98 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF026/99 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF027/00 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF027/01 (skin, fibroblast) - GEIMM
IGF027/77 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF027/78 (skin, fibroblast) - GEIMM
IGF027/80 (skin, fibroblast) - GEIMM
IGF027/82 (skin, fibroblast) - GEIMM
IGF027/83 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF027/84 (skin, fibroblast) - GEIMM
IGF027/85 (skin, fibroblast) - GEIMM
IGF027/86 (skin, fibroblast) - GEIMM
IGF027/87 (skin, fibroblast) - GEIMM
IGF027/88 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF027/89 (skin, fibroblast) - GEIMM
IGF027/90 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF027/91 (skin, fibroblast) - GEIMM
IGF027/92 (skin, fibroblast) - GEIMM
IGF027/93 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF027/94 (skin, fibroblast) - GEIMM
IGF027/95 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF027/96 (skin, fibroblast) - GEIMM
IGF027/97 (skin, fibroblast) - GEIMM
IGF027/98 (skin, fibroblast) - GEIMM
IGF027/99 (skin, fibroblast) - GEIMM
IGF028/00 (skin, fibroblast, spongy degeneration of central nervous system /Canavan disease) - GEIMM
IGF028/01 (skin, fibroblast) - GEIMM
IGF028/77 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF028/78 (skin, fibroblast) - GEIMM
IGF028/80 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF028/81 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF028/82 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF028/83 (skin, fibroblast) - GEIMM
IGF028/84 (skin, fibroblast) - GEIMM
IGF028/85 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF028/86 (skin, fibroblast) - GEIMM
IGF028/87 (skin, fibroblast) - GEIMM
IGF028/88 (skin, fibroblast) - GEIMM
IGF028/89 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF028/91 (skin, fibroblast) - GEIMM
IGF028/92 (skin, fibroblast, sialic acid storage disease) - GEIMM
IGF028/93 (skin, fibroblast) - GEIMM
IGF028/95 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF028/97 (skin, fibroblast) - GEIMM
IGF028/98 (skin, fibroblast, Krabbe disease) - GEIMM
IGF028/99 (skin, fibroblast) - GEIMM
IGF029/00 (skin, fibroblast) - GEIMM
IGF029/01 (skin, fibroblast) - GEIMM
IGF029/77 (skin, fibroblast, arsa pseudodeficiency) - GEIMM
IGF029/78 (skin, fibroblast) - GEIMM
IGF029/81 (skin, fibroblast, homocystinuria) - GEIMM
IGF029/82 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF029/83 (skin, fibroblast, arsa pseudodeficiency) - GEIMM
IGF029/85 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF029/86 (skin, fibroblast) - GEIMM
IGF029/87 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF029/88 (skin, fibroblast) - GEIMM
IGF029/89 (skin, fibroblast) - GEIMM
IGF029/91 (skin, fibroblast) - GEIMM
IGF029/92 (skin, fibroblast, spastic paraparesis) - GEIMM
IGF029/93 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF029/97 (skin, fibroblast) - GEIMM
IGF029/98 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF029/99 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF030/00 (skin, fibroblast) - GEIMM
IGF030/01 (skin, fibroblast) - GEIMM
IGF030/77 (skin, fibroblast) - GEIMM
IGF030/78 (skin, fibroblast) - GEIMM
IGF030/80 (skin, fibroblast) - GEIMM
IGF030/83 (skin, fibroblast) - GEIMM
IGF030/84 (skin, fibroblast) - GEIMM
IGF030/85 (skin, fibroblast) - GEIMM
IGF030/86 (skin, fibroblast) - GEIMM
IGF030/87 (skin, fibroblast) - GEIMM
IGF030/88 (skin, fibroblast) - GEIMM
IGF030/89 (skin, fibroblast) - GEIMM
IGF030/91 (skin, fibroblast) - GEIMM
IGF030/92 (skin, fibroblast) - GEIMM
IGF030/94 (skin, fibroblast) - GEIMM
IGF030/96 (skin, fibroblast) - GEIMM
IGF030/97 (skin, fibroblast) - GEIMM
IGF030/98 (skin, fibroblast) - GEIMM
IGF030/99 (skin, fibroblast) - GEIMM
IGF031/00 (skin, fibroblast, SURF1) - GEIMM
IGF031/01 (skin, fibroblast) - GEIMM
IGF031/77 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF031/80 (skin, fibroblast, mucopolysaccharidosis type III D) - GEIMM
IGF031/81 (skin, fibroblast) - GEIMM
IGF031/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF031/84 (skin, fibroblast) - GEIMM
IGF031/85 (skin, fibroblast, alkaptonuria) - GEIMM
IGF031/86 (skin, fibroblast) - GEIMM
IGF031/88 (skin, fibroblast) - GEIMM
IGF031/89 (skin, fibroblast) - GEIMM
IGF031/90 (skin, fibroblast, osteogenesis imperfecta, type I neurofibr.) - GEIMM
IGF031/91 (skin, fibroblast) - GEIMM
IGF031/92 (skin, fibroblast) - GEIMM
IGF031/93 (skin, fibroblast) - GEIMM
IGF031/94 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF031/96 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF031/97 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF031/98 (skin, fibroblast) - GEIMM
IGF031/99 (skin, fibroblast) - GEIMM
IGF032/00 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF032/01 (skin, fibroblast) - GEIMM
IGF032/76 (skin, fibroblast, neuraminidase deficiency with beta-galactosidase deficiency) - GEIMM
IGF032/77 (skin, fibroblast) - GEIMM
IGF032/78 (skin, fibroblast) - GEIMM
IGF032/80 (skin, fibroblast) - GEIMM
IGF032/81 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF032/82 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF032/83 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF032/84 (skin, fibroblast) - GEIMM
IGF032/85 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF032/86 (skin, fibroblast) - GEIMM
IGF032/87 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF032/88 (skin, fibroblast) - GEIMM
IGF032/89 (skin, fibroblast) - GEIMM
IGF032/90 (skin, fibroblast) - GEIMM
IGF032/91 (skin, fibroblast) - GEIMM
IGF032/93 (skin, fibroblast) - GEIMM
IGF032/94 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF032/96 (skin, fibroblast) - GEIMM
IGF032/97 (skin, fibroblast) - GEIMM
IGF032/98 (skin, fibroblast) - GEIMM
IGF032/99 (skin, fibroblast) - GEIMM
IGF033/00 (skin, fibroblast) - GEIMM
IGF033/01 (skin, fibroblast) - GEIMM
IGF033/77 (skin, fibroblast) - GEIMM
IGF033/78 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF033/80 (skin, fibroblast) - GEIMM
IGF033/81 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF033/83 (skin, fibroblast, fucosidosis) - GEIMM
IGF033/84 (skin, fibroblast) - GEIMM
IGF033/85 (skin, fibroblast) - GEIMM
IGF033/86 (skin, fibroblast, multiple carboxylase deficiency, biotin-responsive) - GEIMM
IGF033/87 (skin, fibroblast) - GEIMM
IGF033/88 (skin, fibroblast) - GEIMM
IGF033/89 (skin, fibroblast, sensorineural deafness) - GEIMM
IGF033/90 (skin, fibroblast, COFS syndrome / cerebrooculofacioskeletal syndrome) - GEIMM
IGF033/91 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF033/93 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF033/94 (skin, fibroblast) - GEIMM
IGF033/95 (skin, fibroblast) - GEIMM
IGF033/96 (skin, fibroblast) - GEIMM
IGF033/97 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF033/98 (skin, fibroblast) - GEIMM
IGF033/99 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF034/00 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF034/01 (skin, fibroblast) - GEIMM
IGF034/76 (skin, fibroblast, SCID (severe combined immunodeficiency 1)) - GEIMM
IGF034/77 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF034/80 (skin, fibroblast) - GEIMM
IGF034/81 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF034/83 (skin, fibroblast) - GEIMM
IGF034/84 (skin, fibroblast) - GEIMM
IGF034/85 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF034/86 (skin, fibroblast) - GEIMM
IGF034/87 (skin, fibroblast) - GEIMM
IGF034/88 (skin, fibroblast) - GEIMM
IGF034/89 (skin, fibroblast) - GEIMM
IGF034/90 (skin, fibroblast) - GEIMM
IGF034/91 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF034/92 (skin, fibroblast) - GEIMM
IGF034/93 (skin, fibroblast) - GEIMM
IGF034/94 (skin, fibroblast) - GEIMM
IGF034/95 (skin, fibroblast) - GEIMM
IGF034/96 (skin, fibroblast) - GEIMM
IGF034/97 (skin, fibroblast, argininosuccinicaciduria) - GEIMM
IGF034/98 (skin, fibroblast) - GEIMM
IGF034/99 (skin, fibroblast) - GEIMM
IGF035/00 (skin, fibroblast) - GEIMM
IGF035/01 (skin, fibroblast) - GEIMM
IGF035/77 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF035/80 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF035/81 (skin, fibroblast, fucosidosis) - GEIMM
IGF035/82 (skin, fibroblast) - GEIMM
IGF035/83 (skin, fibroblast) - GEIMM
IGF035/85 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF035/86 (skin, fibroblast) - GEIMM
IGF035/87 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF035/88 (skin, fibroblast, fucosidosis) - GEIMM
IGF035/89 (skin, fibroblast) - GEIMM
IGF035/90 (skin, fibroblast) - GEIMM
IGF035/91 (skin, fibroblast) - GEIMM
IGF035/92 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF035/93 (skin, fibroblast) - GEIMM
IGF035/94 (skin, fibroblast, mucolipidosis III) - GEIMM
IGF035/96 (skin, fibroblast) - GEIMM
IGF035/97 (skin, fibroblast) - GEIMM
IGF035/98 (skin, fibroblast) - GEIMM
IGF035/99 (skin, fibroblast) - GEIMM
IGF036/00 (skin, fibroblast, Krabbe disease) - GEIMM
IGF036/01 (skin, fibroblast) - GEIMM
IGF036/76 (skin, fibroblast) - GEIMM
IGF036/77 (skin, fibroblast) - GEIMM
IGF036/78 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF036/79 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF036/80 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF036/81 (skin, fibroblast) - GEIMM
IGF036/83 (skin, fibroblast, Krabbe disease) - GEIMM
IGF036/84 (skin, fibroblast) - GEIMM
IGF036/86 (skin, fibroblast) - GEIMM
IGF036/87 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF036/88 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF036/89 (skin, fibroblast) - GEIMM
IGF036/90 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF036/92 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF036/93 (skin, fibroblast) - GEIMM
IGF036/94 (skin, fibroblast) - GEIMM
IGF036/96 (skin, fibroblast) - GEIMM
IGF036/97 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF036/98 (skin, fibroblast) - GEIMM
IGF036/99 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF037/00 (skin, fibroblast) - GEIMM
IGF037/01 (skin, fibroblast) - GEIMM
IGF037/76 (skin, fibroblast) - GEIMM
IGF037/77 (skin, fibroblast) - GEIMM
IGF037/78 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF037/80 (skin, fibroblast) - GEIMM
IGF037/82 (skin, fibroblast) - GEIMM
IGF037/83 (skin, fibroblast) - GEIMM
IGF037/84 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF037/85 (skin, fibroblast) - GEIMM
IGF037/86 (skin, fibroblast, myopathy with deficiency of CPT I) - GEIMM
IGF037/87 (skin, fibroblast) - GEIMM
IGF037/91 (skin, fibroblast) - GEIMM
IGF037/92 (skin, fibroblast) - GEIMM
IGF037/93 (skin, fibroblast) - GEIMM
IGF037/94 (skin, fibroblast, aspartylglycosaminuria) - GEIMM
IGF037/95 (skin, fibroblast, molybdenum cofactor deficiency) - GEIMM
IGF037/97 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF037/98 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF037/99 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF038/00 (skin, fibroblast) - GEIMM
IGF038/01 (skin, fibroblast) - GEIMM
IGF038/80 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF038/81 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF038/82 (skin, fibroblast) - GEIMM
IGF038/83 (skin, fibroblast) - GEIMM
IGF038/84 (skin, fibroblast) - GEIMM
IGF038/85 (skin, fibroblast) - GEIMM
IGF038/86 (skin, fibroblast, Roberts syndrome) - GEIMM
IGF038/87 (skin, fibroblast) - GEIMM
IGF038/88 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF038/89 (skin, fibroblast, isovalericacidemia) - GEIMM
IGF038/90 (skin, fibroblast) - GEIMM
IGF038/91 (skin, fibroblast, Charcot-Marie-Tooth disease) - GEIMM
IGF038/92 (skin, fibroblast) - GEIMM
IGF038/93 (skin, fibroblast, Turner syndrome, mosaic) - GEIMM
IGF038/95 (skin, fibroblast, encephalomyopaty mitocondrial) - GEIMM
IGF038/96 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF038/97 (skin, fibroblast) - GEIMM
IGF038/98 (skin, fibroblast) - GEIMM
IGF038/99 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF039/00 (skin, fibroblast) - GEIMM
IGF039/01 (skin, fibroblast) - GEIMM
IGF039/77 (skin, fibroblast) - GEIMM
IGF039/80 (skin, fibroblast) - GEIMM
IGF039/81 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF039/82 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF039/83 (skin, fibroblast) - GEIMM
IGF039/84 (skin, fibroblast) - GEIMM
IGF039/85 (skin, fibroblast, Ehlers-Danlos syndrome) - GEIMM
IGF039/86 (skin, fibroblast) - GEIMM
IGF039/87 (skin, fibroblast) - GEIMM
IGF039/88 (skin, fibroblast) - GEIMM
IGF039/90 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF039/91 (skin, fibroblast, Angelman syndrome) - GEIMM
IGF039/92 (skin, fibroblast) - GEIMM
IGF039/93 (skin, fibroblast, histiocytosis X) - GEIMM
IGF039/94 (skin, fibroblast) - GEIMM
IGF039/95 (skin, fibroblast) - GEIMM
IGF039/96 (skin, fibroblast) - GEIMM
IGF039/97 (skin, fibroblast) - GEIMM
IGF039/98 (skin, fibroblast) - GEIMM
IGF039/99 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF040/00 (skin, fibroblast) - GEIMM
IGF040/01 (skin, fibroblast) - GEIMM
IGF040/77 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF040/78 (skin, fibroblast) - GEIMM
IGF040/79 (skin, fibroblast) - GEIMM
IGF040/80 (skin, fibroblast) - GEIMM
IGF040/82 (skin, fibroblast) - GEIMM
IGF040/83 (skin, fibroblast) - GEIMM
IGF040/84 (skin, fibroblast) - GEIMM
IGF040/85 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF040/86 (skin, fibroblast) - GEIMM
IGF040/87 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF040/89 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF040/90 (skin, fibroblast, Krabbe disease) - GEIMM
IGF040/91 (skin, fibroblast) - GEIMM
IGF040/92 (skin, fibroblast) - GEIMM
IGF040/93 (skin, fibroblast) - GEIMM
IGF040/94 (skin, fibroblast) - GEIMM
IGF040/95 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF040/96 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF040/97 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - GEIMM
IGF040/98 (skin, fibroblast) - GEIMM
IGF040/99 (skin, fibroblast) - GEIMM
IGF041/00 (skin, fibroblast) - GEIMM
IGF041/01 (skin, fibroblast) - GEIMM
IGF041/77 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF041/78 (skin, fibroblast) - GEIMM
IGF041/80 (skin, fibroblast, ichthyosis X-linked) - GEIMM
IGF041/81 (skin, fibroblast) - GEIMM
IGF041/84 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF041/85 (skin, fibroblast) - GEIMM
IGF041/86 (skin, fibroblast, hyperglycerolemia) - GEIMM
IGF041/87 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF041/88 (skin, fibroblast) - GEIMM
IGF041/89 (skin, fibroblast) - GEIMM
IGF041/90 (skin, fibroblast, geleophysic dwarfism) - GEIMM
IGF041/91 (skin, fibroblast) - GEIMM
IGF041/92 (skin, fibroblast) - GEIMM
IGF041/94 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF041/95 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF041/96 (skin, fibroblast) - GEIMM
IGF041/97 (skin, fibroblast) - GEIMM
IGF041/98 (skin, fibroblast) - GEIMM
IGF041/99 (skin, fibroblast) - GEIMM
IGF042/00 (skin, fibroblast) - GEIMM
IGF042/01 (skin, fibroblast) - GEIMM
IGF042/77 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF042/80 (skin, fibroblast) - GEIMM
IGF042/81 (skin, fibroblast) - GEIMM
IGF042/82 (skin, fibroblast) - GEIMM
IGF042/83 (skin, fibroblast) - GEIMM
IGF042/84 (skin, fibroblast) - GEIMM
IGF042/85 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF042/86 (skin, fibroblast) - GEIMM
IGF042/87 (skin, fibroblast) - GEIMM
IGF042/88 (skin, fibroblast) - GEIMM
IGF042/89 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF042/90 (skin, fibroblast, encephalopathy) - GEIMM
IGF042/91 (skin, fibroblast) - GEIMM
IGF042/92 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF042/93 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF042/94 (skin, fibroblast, Krabbe disease) - GEIMM
IGF042/95 (skin, fibroblast) - GEIMM
IGF042/96 (skin, fibroblast) - GEIMM
IGF042/97 (skin, fibroblast) - GEIMM
IGF042/98 (skin, fibroblast) - GEIMM
IGF042/99 (skin, fibroblast) - GEIMM
IGF043/00 (skin, fibroblast) - GEIMM
IGF043/77 (skin, fibroblast) - GEIMM
IGF043/78 (skin, fibroblast, ichthyosis X-linked) - GEIMM
IGF043/79 (skin, fibroblast) - GEIMM
IGF043/80 (skin, fibroblast) - GEIMM
IGF043/81 (skin, fibroblast) - GEIMM
IGF043/82 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF043/84 (skin, fibroblast) - GEIMM
IGF043/85 (skin, fibroblast) - GEIMM
IGF043/86 (skin, fibroblast) - GEIMM
IGF043/88 (skin, fibroblast) - GEIMM
IGF043/89 (skin, fibroblast) - GEIMM
IGF043/90 (skin, fibroblast) - GEIMM
IGF043/91 (skin, fibroblast, arsa pseudodeficiency) - GEIMM
IGF043/92 (skin, fibroblast) - GEIMM
IGF043/93 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF043/94 (skin, fibroblast) - GEIMM
IGF043/96 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF043/97 (skin, fibroblast) - GEIMM
IGF043/98 (skin, fibroblast) - GEIMM
IGF043/99 (skin, fibroblast) - GEIMM
IGF044/00 (skin, fibroblast) - GEIMM
IGF044/77 (skin, fibroblast) - GEIMM
IGF044/78 (skin, fibroblast) - GEIMM
IGF044/79 (skin, fibroblast) - GEIMM
IGF044/81 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF044/82 (skin, fibroblast) - GEIMM
IGF044/83 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF044/84 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF044/85 (skin, fibroblast) - GEIMM
IGF044/86 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF044/87 (skin, fibroblast) - GEIMM
IGF044/88 (skin, fibroblast) - GEIMM
IGF044/89 (skin, fibroblast) - GEIMM
IGF044/90 (skin, fibroblast) - GEIMM
IGF044/91 (skin, fibroblast) - GEIMM
IGF044/92 (skin, fibroblast) - GEIMM
IGF044/93 (skin, fibroblast) - GEIMM
IGF044/94 (skin, fibroblast) - GEIMM
IGF044/95 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF044/96 (skin, fibroblast) - GEIMM
IGF044/97 (skin, fibroblast) - GEIMM
IGF044/98 (skin, fibroblast) - GEIMM
IGF044/99 (skin, fibroblast) - GEIMM
IGF045/00 (skin, fibroblast) - GEIMM
IGF045/78 (skin, fibroblast) - GEIMM
IGF045/79 (skin, fibroblast, mucolipidosis III) - GEIMM
IGF045/80 (skin, fibroblast) - GEIMM
IGF045/81 (skin, fibroblast) - GEIMM
IGF045/82 (skin, fibroblast) - GEIMM
IGF045/83 (skin, fibroblast) - GEIMM
IGF045/84 (skin, fibroblast) - GEIMM
IGF045/85 (skin, fibroblast) - GEIMM
IGF045/86 (skin, fibroblast) - GEIMM
IGF045/87 (skin, fibroblast) - GEIMM
IGF045/88 (skin, fibroblast) - GEIMM
IGF045/89 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF045/90 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF045/91 (skin, fibroblast) - GEIMM
IGF045/92 (skin, fibroblast) - GEIMM
IGF045/93 (skin, fibroblast) - GEIMM
IGF045/94 (skin, fibroblast) - GEIMM
IGF045/95 (skin, fibroblast) - GEIMM
IGF045/96 (skin, fibroblast) - GEIMM
IGF045/97 (skin, fibroblast) - GEIMM
IGF045/98 (skin, fibroblast) - GEIMM
IGF045/99 (skin, fibroblast) - GEIMM
IGF046/00 (skin, fibroblast) - GEIMM
IGF046/76 (skin, fibroblast) - GEIMM
IGF046/78 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF046/79 (skin, fibroblast) - GEIMM
IGF046/80 (skin, fibroblast) - GEIMM
IGF046/81 (skin, fibroblast) - GEIMM
IGF046/82 (skin, fibroblast, Coffin-Lowry syndrome) - GEIMM
IGF046/83 (skin, fibroblast) - GEIMM
IGF046/84 (skin, fibroblast) - GEIMM
IGF046/85 (skin, fibroblast) - GEIMM
IGF046/87 (skin, fibroblast) - GEIMM
IGF046/89 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF046/90 (skin, fibroblast, Krabbe disease) - GEIMM
IGF046/91 (skin, fibroblast) - GEIMM
IGF046/92 (skin, fibroblast, dystrophy congenital progressive) - GEIMM
IGF046/93 (skin, fibroblast) - GEIMM
IGF046/94 (skin, fibroblast) - GEIMM
IGF046/95 (skin, fibroblast, Costello syndrome) - GEIMM
IGF046/96 (skin, fibroblast) - GEIMM
IGF046/97 (skin, fibroblast) - GEIMM
IGF046/98 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF046/99 (skin, fibroblast) - GEIMM
IGF047/00 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF047/78 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF047/80 (skin, fibroblast) - GEIMM
IGF047/82 (skin, fibroblast, phenylketonuria II) - GEIMM
IGF047/83 (skin, fibroblast) - GEIMM
IGF047/84 (skin, fibroblast) - GEIMM
IGF047/85 (skin, fibroblast) - GEIMM
IGF047/86 (skin, fibroblast) - GEIMM
IGF047/87 (skin, fibroblast) - GEIMM
IGF047/88 (skin, fibroblast) - GEIMM
IGF047/89 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF047/90 (skin, fibroblast) - GEIMM
IGF047/91 (skin, fibroblast) - GEIMM
IGF047/92 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF047/94 (skin, fibroblast) - GEIMM
IGF047/95 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF047/96 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF047/97 (skin, fibroblast) - GEIMM
IGF047/98 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF047/99 (skin, fibroblast) - GEIMM
IGF048/77 (skin, fibroblast) - GEIMM
IGF048/79 (skin, fibroblast) - GEIMM
IGF048/80 (skin, fibroblast, aspartylglycosaminuria) - GEIMM
IGF048/82 (skin, fibroblast, galactosemia) - GEIMM
IGF048/83 (skin, fibroblast) - GEIMM
IGF048/84 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF048/85 (skin, fibroblast) - GEIMM
IGF048/86 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF048/89 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF048/90 (skin, fibroblast) - GEIMM
IGF048/91 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF048/94 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF048/95 (skin, fibroblast) - GEIMM
IGF048/96 (skin, fibroblast, muscolar dystrophy def.sarcoglican) - GEIMM
IGF048/97 (skin, fibroblast) - GEIMM
IGF048/98 (skin, fibroblast) - GEIMM
IGF048/99 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF049/00 (skin, fibroblast) - GEIMM
IGF049/77 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF049/78 (skin, fibroblast) - GEIMM
IGF049/79 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF049/80 (skin, fibroblast) - GEIMM
IGF049/82 (skin, fibroblast) - GEIMM
IGF049/83 (skin, fibroblast) - GEIMM
IGF049/84 (skin, fibroblast) - GEIMM
IGF049/85 (skin, fibroblast) - GEIMM
IGF049/86 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF049/87 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF049/89 (skin, fibroblast, homocystinuria) - GEIMM
IGF049/90 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF049/91 (skin, fibroblast, hypercholesterolemia, familial) - GEIMM
IGF049/92 (skin, fibroblast) - GEIMM
IGF049/93 (skin, fibroblast, Krabbe disease) - GEIMM
IGF049/94 (skin, fibroblast) - GEIMM
IGF049/95 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF049/96 (skin, fibroblast, SCID (severe combined immunodeficiency 1)) - GEIMM
IGF049/97 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF049/98 (skin, fibroblast) - GEIMM
IGF049/99 (skin, fibroblast, methylenetetra-hydrofolate reductase def.) - GEIMM
IGF050/00 (skin, fibroblast, Costello syndrome) - GEIMM
IGF050/76 (skin, fibroblast, fructose intolerance, hereditary) - GEIMM
IGF050/77 (skin, fibroblast) - GEIMM
IGF050/78 (skin, fibroblast) - GEIMM
IGF050/80 (skin, fibroblast) - GEIMM
IGF050/83 (skin, fibroblast) - GEIMM
IGF050/84 (skin, fibroblast) - GEIMM
IGF050/85 (skin, fibroblast) - GEIMM
IGF050/86 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF050/87 (skin, fibroblast) - GEIMM
IGF050/90 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF050/91 (skin, fibroblast) - GEIMM
IGF050/92 (skin, fibroblast, Aicardi syndrome / corpus callosum) - GEIMM
IGF050/93 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF050/97 (skin, fibroblast) - GEIMM
IGF050/98 (skin, fibroblast) - GEIMM
IGF050/99 (skin, fibroblast) - GEIMM
IGF051/00 (skin, fibroblast) - GEIMM
IGF051/77 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF051/78 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF051/80 (skin, fibroblast) - GEIMM
IGF051/82 (skin, fibroblast, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF051/83 (skin, fibroblast) - GEIMM
IGF051/84 (skin, fibroblast) - GEIMM
IGF051/85 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - GEIMM
IGF051/86 (skin, fibroblast) - GEIMM
IGF051/87 (skin, fibroblast) - GEIMM
IGF051/88 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF051/89 (skin, fibroblast) - GEIMM
IGF051/90 (skin, fibroblast) - GEIMM
IGF051/91 (skin, fibroblast, dibasicaminoaciduria II) - GEIMM
IGF051/92 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF051/93 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF051/94 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF051/95 (skin, fibroblast) - GEIMM
IGF051/97 (skin, fibroblast, pycnodysostosis) - GEIMM
IGF051/98 (skin, fibroblast) - GEIMM
IGF051/99 (skin, fibroblast) - GEIMM
IGF052/00 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF052/76 (skin, fibroblast) - GEIMM
IGF052/77 (skin, fibroblast) - GEIMM
IGF052/78 (skin, fibroblast) - GEIMM
IGF052/80 (skin, fibroblast) - GEIMM
IGF052/81 (skin, fibroblast) - GEIMM
IGF052/82 (skin, fibroblast) - GEIMM
IGF052/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF052/84 (skin, fibroblast) - GEIMM
IGF052/85 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - GEIMM
IGF052/86 (skin, fibroblast, ataxia telangiectasia) - GEIMM
IGF052/87 (skin, fibroblast) - GEIMM
IGF052/88 (skin, fibroblast) - GEIMM
IGF052/89 (skin, fibroblast, hemochromatosis neonatal) - GEIMM
IGF052/90 (skin, fibroblast) - GEIMM
IGF052/91 (skin, fibroblast) - GEIMM
IGF052/92 (skin, fibroblast) - GEIMM
IGF052/93 (skin, fibroblast, Costello syndrome) - GEIMM
IGF052/94 (skin, fibroblast) - GEIMM
IGF052/95 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF052/97 (skin, fibroblast) - GEIMM
IGF052/99 (skin, fibroblast) - GEIMM
IGF053/00 (skin, fibroblast) - GEIMM
IGF053/78 (skin, fibroblast) - GEIMM
IGF053/80 (skin, fibroblast) - GEIMM
IGF053/81 (skin, fibroblast) - GEIMM
IGF053/83 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF053/84 (skin, fibroblast) - GEIMM
IGF053/85 (skin, fibroblast) - GEIMM
IGF053/86 (skin, fibroblast) - GEIMM
IGF053/87 (skin, fibroblast) - GEIMM
IGF053/89 (skin, fibroblast) - GEIMM
IGF053/90 (skin, fibroblast) - GEIMM
IGF053/91 (skin, fibroblast) - GEIMM
IGF053/92 (skin, fibroblast) - GEIMM
IGF053/94 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF053/97 (skin, fibroblast) - GEIMM
IGF053/99 (skin, fibroblast) - GEIMM
IGF054/77 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF054/78 (skin, fibroblast) - GEIMM
IGF054/80 (skin, fibroblast) - GEIMM
IGF054/82 (skin, fibroblast) - GEIMM
IGF054/83 (skin, fibroblast) - GEIMM
IGF054/84 (skin, fibroblast) - GEIMM
IGF054/85 (skin, fibroblast) - GEIMM
IGF054/86 (skin, fibroblast) - GEIMM
IGF054/89 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF054/90 (skin, fibroblast) - GEIMM
IGF054/91 (skin, fibroblast, dibasicaminoaciduria II) - GEIMM
IGF054/92 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF054/93 (skin, fibroblast, fucosidosis) - GEIMM
IGF054/94 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF054/95 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF054/97 (skin, fibroblast, pycnodysostosis) - GEIMM
IGF054/99 (skin, fibroblast) - GEIMM
IGF055/77 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF055/78 (skin, fibroblast) - GEIMM
IGF055/80 (skin, fibroblast) - GEIMM
IGF055/83 (skin, fibroblast) - GEIMM
IGF055/84 (skin, fibroblast) - GEIMM
IGF055/86 (skin, fibroblast) - GEIMM
IGF055/87 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF055/88 (skin, fibroblast, factor XIII deficiency) - GEIMM
IGF055/89 (skin, fibroblast, trisomy 21 / Down syndrome) - GEIMM
IGF055/90 (skin, fibroblast) - GEIMM
IGF055/92 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF055/93 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF055/94 (skin, fibroblast) - GEIMM
IGF055/95 (skin, fibroblast) - GEIMM
IGF055/97 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF055/99 (skin, fibroblast) - GEIMM
IGF056/78 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF056/79 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF056/80 (skin, fibroblast) - GEIMM
IGF056/81 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF056/82 (skin, fibroblast) - GEIMM
IGF056/83 (skin, fibroblast) - GEIMM
IGF056/85 (skin, fibroblast) - GEIMM
IGF056/87 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF056/90 (skin, fibroblast) - GEIMM
IGF056/91 (skin, fibroblast, chondrodysplasia punctata) - GEIMM
IGF056/92 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF056/93 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF056/94 (skin, fibroblast) - GEIMM
IGF056/95 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF056/97 (skin, fibroblast) - GEIMM
IGF057/76 (skin, fibroblast) - GEIMM
IGF057/77 (skin, fibroblast) - GEIMM
IGF057/78 (skin, fibroblast) - GEIMM
IGF057/80 (skin, fibroblast) - GEIMM
IGF057/81 (skin, fibroblast) - GEIMM
IGF057/82 (skin, fibroblast) - GEIMM
IGF057/83 (skin, fibroblast) - GEIMM
IGF057/84 (skin, fibroblast) - GEIMM
IGF057/85 (skin, fibroblast) - GEIMM
IGF057/86 (skin, fibroblast) - GEIMM
IGF057/87 (skin, fibroblast) - GEIMM
IGF057/88 (skin, fibroblast) - GEIMM
IGF057/89 (skin, fibroblast) - GEIMM
IGF057/90 (skin, fibroblast) - GEIMM
IGF057/91 (skin, fibroblast, Ehlers-Danlos syndrome, type I) - GEIMM
IGF057/92 (skin, fibroblast, Zellweger syndrome) - GEIMM
IGF057/93 (skin, fibroblast) - GEIMM
IGF057/95 (skin, fibroblast) - GEIMM
IGF057/97 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF058/78 (skin, fibroblast) - GEIMM
IGF058/79 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF058/80 (skin, fibroblast) - GEIMM
IGF058/82 (skin, fibroblast) - GEIMM
IGF058/83 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF058/84 (skin, fibroblast) - GEIMM
IGF058/85 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF058/86 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF058/87 (skin, fibroblast) - GEIMM
IGF058/89 (skin, fibroblast) - GEIMM
IGF058/90 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF058/91 (skin, fibroblast) - GEIMM
IGF058/93 (skin, fibroblast) - GEIMM
IGF058/95 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF058/97 (skin, fibroblast) - GEIMM
IGF059/76 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF059/78 (skin, fibroblast) - GEIMM
IGF059/79 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF059/80 (skin, fibroblast, Fanconi anemia, type I) - GEIMM
IGF059/82 (skin, fibroblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF059/83 (skin, fibroblast) - GEIMM
IGF059/84 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF059/85 (skin, fibroblast) - GEIMM
IGF059/86 (skin, fibroblast) - GEIMM
IGF059/87 (skin, fibroblast) - GEIMM
IGF059/89 (skin, fibroblast) - GEIMM
IGF059/90 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF059/91 (skin, fibroblast) - GEIMM
IGF059/92 (skin, fibroblast) - GEIMM
IGF059/93 (skin, fibroblast) - GEIMM
IGF059/95 (skin, fibroblast) - GEIMM
IGF059/97 (skin, fibroblast) - GEIMM
IGF060/78 (skin, fibroblast, proteolipid protein, myelin) - GEIMM
IGF060/79 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF060/80 (skin, fibroblast) - GEIMM
IGF060/81 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF060/82 (skin, fibroblast, fibromatosis, juvenile hyaline) - GEIMM
IGF060/83 (skin, fibroblast) - GEIMM
IGF060/84 (skin, fibroblast, hyperglycinemia, nonketotic) - GEIMM
IGF060/86 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF060/87 (skin, fibroblast) - GEIMM
IGF060/88 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF060/89 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF060/90 (skin, fibroblast) - GEIMM
IGF060/91 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF060/92 (skin, fibroblast) - GEIMM
IGF060/93 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF060/95 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF060/97 (skin, fibroblast, Krabbe disease) - GEIMM
IGF061/76 (skin, fibroblast) - GEIMM
IGF061/78 (skin, fibroblast) - GEIMM
IGF061/79 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF061/81 (skin, fibroblast, Hallervorden-Spatz disease) - GEIMM
IGF061/82 (skin, fibroblast) - GEIMM
IGF061/83 (skin, fibroblast) - GEIMM
IGF061/84 (skin, fibroblast) - GEIMM
IGF061/85 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF061/86 (skin, fibroblast) - GEIMM
IGF061/87 (skin, fibroblast) - GEIMM
IGF061/88 (skin, fibroblast) - GEIMM
IGF061/89 (skin, fibroblast) - GEIMM
IGF061/90 (skin, fibroblast) - GEIMM
IGF061/91 (skin, fibroblast) - GEIMM
IGF061/92 (skin, fibroblast) - GEIMM
IGF061/93 (skin, fibroblast) - GEIMM
IGF061/95 (skin, fibroblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF061/97 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF062/78 (skin, fibroblast) - GEIMM
IGF062/79 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF062/81 (skin, fibroblast) - GEIMM
IGF062/82 (skin, fibroblast) - GEIMM
IGF062/83 (skin, fibroblast) - GEIMM
IGF062/84 (skin, fibroblast) - GEIMM
IGF062/85 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF062/86 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF062/87 (skin, fibroblast) - GEIMM
IGF062/88 (skin, fibroblast) - GEIMM
IGF062/89 (skin, fibroblast, neuraminidase deficiency with beta-galactosidase deficiency) - GEIMM
IGF062/90 (skin, fibroblast, Costello syndrome) - GEIMM
IGF062/91 (skin, fibroblast) - GEIMM
IGF062/95 (skin, fibroblast, Glutaricacidemia I) - GEIMM
IGF062/97 (skin, fibroblast) - GEIMM
IGF063/76 (skin, fibroblast) - GEIMM
IGF063/77 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF063/78 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF063/79 (skin, fibroblast) - GEIMM
IGF063/80 (skin, fibroblast) - GEIMM
IGF063/81 (skin, fibroblast) - GEIMM
IGF063/82 (skin, fibroblast) - GEIMM
IGF063/84 (skin, fibroblast) - GEIMM
IGF063/85 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF063/86 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF063/87 (skin, fibroblast) - GEIMM
IGF063/90 (skin, fibroblast) - GEIMM
IGF063/91 (skin, fibroblast) - GEIMM
IGF063/93 (skin, fibroblast) - GEIMM
IGF063/95 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF063/96 (skin, fibroblast) - GEIMM
IGF064/76 (skin, fibroblast) - GEIMM
IGF064/78 (skin, fibroblast) - GEIMM
IGF064/79 (skin, fibroblast) - GEIMM
IGF064/80 (skin, fibroblast) - GEIMM
IGF064/81 (skin, fibroblast, Wilson disease) - GEIMM
IGF064/82 (skin, fibroblast) - GEIMM
IGF064/83 (skin, fibroblast) - GEIMM
IGF064/84 (skin, fibroblast) - GEIMM
IGF064/85 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF064/86 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF064/87 (skin, fibroblast) - GEIMM
IGF064/88 (skin, fibroblast) - GEIMM
IGF064/89 (skin, fibroblast) - GEIMM
IGF064/90 (skin, fibroblast) - GEIMM
IGF064/91 (skin, fibroblast) - GEIMM
IGF064/93 (skin, fibroblast) - GEIMM
IGF064/95 (skin, fibroblast) - GEIMM
IGF065/77 (skin, fibroblast) - GEIMM
IGF065/79 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF065/80 (skin, fibroblast) - GEIMM
IGF065/81 (skin, fibroblast) - GEIMM
IGF065/83 (skin, fibroblast) - GEIMM
IGF065/84 (skin, fibroblast) - GEIMM
IGF065/86 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF065/87 (skin, fibroblast) - GEIMM
IGF065/88 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF065/90 (skin, fibroblast, testicular feminization syndrome) - GEIMM
IGF065/91 (skin, fibroblast, Ehlers-Danlos syndrome) - GEIMM
IGF065/92 (skin, fibroblast, Sjogren-Larsson syndrome) - GEIMM
IGF065/93 (skin, fibroblast, mitochondrial respiratory chain complex I) - GEIMM
IGF065/95 (skin, fibroblast) - GEIMM
IGF066/76 (skin, fibroblast) - GEIMM
IGF066/77 (skin, fibroblast) - GEIMM
IGF066/78 (skin, fibroblast) - GEIMM
IGF066/79 (skin, fibroblast) - GEIMM
IGF066/80 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF066/82 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF066/83 (skin, fibroblast) - GEIMM
IGF066/84 (skin, fibroblast, homocystinuria) - GEIMM
IGF066/85 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF066/86 (skin, fibroblast) - GEIMM
IGF066/87 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF066/88 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF066/89 (skin, fibroblast) - GEIMM
IGF066/90 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF066/91 (skin, fibroblast, carboydrate deficient glycoprotein syndrome, type I) - GEIMM
IGF066/92 (skin, fibroblast) - GEIMM
IGF066/93 (skin, fibroblast) - GEIMM
IGF066/95 (skin, fibroblast) - GEIMM
IGF067/78 (skin, fibroblast) - GEIMM
IGF067/81 (skin, fibroblast) - GEIMM
IGF067/82 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF067/83 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF067/84 (skin, fibroblast, arsa pseudodeficiency) - GEIMM
IGF067/85 (skin, fibroblast) - GEIMM
IGF067/86 (skin, fibroblast) - GEIMM
IGF067/87 (skin, fibroblast, arthrogryposis multiplex congenita) - GEIMM
IGF067/88 (skin, fibroblast) - GEIMM
IGF067/89 (skin, fibroblast) - GEIMM
IGF067/90 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF067/91 (skin, fibroblast, Zellweger syndrome) - GEIMM
IGF067/92 (skin, fibroblast) - GEIMM
IGF067/93 (skin, fibroblast) - GEIMM
IGF067/95 (skin, fibroblast) - GEIMM
IGF068/78 (skin, fibroblast) - GEIMM
IGF068/79 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF068/80 (skin, fibroblast) - GEIMM
IGF068/82 (skin, fibroblast, Aldrich syndrome) - GEIMM
IGF068/83 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF068/84 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF068/85 (skin, fibroblast) - GEIMM
IGF068/86 (skin, fibroblast) - GEIMM
IGF068/87 (skin, fibroblast) - GEIMM
IGF068/88 (skin, fibroblast) - GEIMM
IGF068/89 (skin, fibroblast, post-traumatic osteoporosis) - GEIMM
IGF068/90 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF068/91 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF068/92 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF068/93 (skin, fibroblast) - GEIMM
IGF068/95 (skin, fibroblast) - GEIMM
IGF069/78 (skin, fibroblast) - GEIMM
IGF069/80 (skin, fibroblast) - GEIMM
IGF069/82 (skin, fibroblast) - GEIMM
IGF069/84 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF069/85 (skin, fibroblast) - GEIMM
IGF069/86 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF069/87 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF069/88 (skin, fibroblast) - GEIMM
IGF069/89 (skin, fibroblast) - GEIMM
IGF069/90 (skin, fibroblast) - GEIMM
IGF069/91 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF069/92 (skin, fibroblast) - GEIMM
IGF069/93 (skin, fibroblast) - GEIMM
IGF069/95 (skin, fibroblast) - GEIMM
IGF070/76 (skin, fibroblast) - GEIMM
IGF070/78 (skin, fibroblast) - GEIMM
IGF070/80 (skin, fibroblast) - GEIMM
IGF070/81 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF070/82 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF070/83 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF070/84 (skin, fibroblast) - GEIMM
IGF070/85 (skin, fibroblast) - GEIMM
IGF070/86 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF070/87 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF070/88 (skin, fibroblast, pyruvate dehydrogenase def.) - GEIMM
IGF070/89 (skin, fibroblast, Edwards' syndrome / trisomy 18) - GEIMM
IGF070/90 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF070/91 (skin, fibroblast) - GEIMM
IGF070/92 (skin, fibroblast) - GEIMM
IGF070/93 (skin, fibroblast) - GEIMM
IGF070/95 (skin, fibroblast) - GEIMM
IGF071/76 (skin, fibroblast) - GEIMM
IGF071/78 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - GEIMM
IGF071/80 (skin, fibroblast) - GEIMM
IGF071/81 (skin, fibroblast) - GEIMM
IGF071/82 (skin, fibroblast) - GEIMM
IGF071/83 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF071/84 (skin, fibroblast) - GEIMM
IGF071/85 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF071/86 (skin, fibroblast) - GEIMM
IGF071/87 (skin, fibroblast) - GEIMM
IGF071/88 (skin, fibroblast) - GEIMM
IGF071/89 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF071/90 (skin, fibroblast) - GEIMM
IGF071/92 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF071/93 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF071/95 (skin, fibroblast, metachromatic leukodystrophy) - GEIMM
IGF072/76 (skin, fibroblast) - GEIMM
IGF072/77 (skin, fibroblast) - GEIMM
IGF072/78 (skin, fibroblast) - GEIMM
IGF072/81 (skin, fibroblast) - GEIMM
IGF072/82 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF072/83 (skin, fibroblast, homocystinuria) - GEIMM
IGF072/84 (skin, fibroblast) - GEIMM
IGF072/85 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF072/86 (skin, fibroblast) - GEIMM
IGF072/87 (skin, fibroblast) - GEIMM
IGF072/88 (skin, fibroblast) - GEIMM
IGF072/89 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF072/90 (skin, fibroblast) - GEIMM
IGF072/91 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF072/92 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF072/95 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF073/76 (skin, fibroblast) - GEIMM
IGF073/78 (skin, fibroblast) - GEIMM
IGF073/82 (skin, fibroblast) - GEIMM
IGF073/83 (skin, fibroblast) - GEIMM
IGF073/84 (skin, fibroblast) - GEIMM
IGF073/85 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - GEIMM
IGF073/86 (skin, fibroblast) - GEIMM
IGF073/87 (skin, fibroblast) - GEIMM
IGF073/88 (skin, fibroblast) - GEIMM
IGF073/89 (skin, fibroblast) - GEIMM
IGF073/90 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF073/91 (skin, fibroblast, geroderma osteodysplastica) - GEIMM
IGF073/92 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF073/95 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF074/76 (skin, fibroblast, triglyceride storage disease) - GEIMM
IGF074/78 (skin, fibroblast, Laurence-Moon syndrome) - GEIMM
IGF074/79 (skin, fibroblast) - GEIMM
IGF074/81 (skin, fibroblast) - GEIMM
IGF074/82 (skin, fibroblast) - GEIMM
IGF074/83 (skin, fibroblast) - GEIMM
IGF074/84 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF074/86 (skin, fibroblast) - GEIMM
IGF074/87 (skin, fibroblast) - GEIMM
IGF074/88 (skin, fibroblast) - GEIMM
IGF074/89 (skin, fibroblast, Ellis-Van Creveld syndrome) - GEIMM
IGF074/90 (skin, fibroblast) - GEIMM
IGF074/92 (skin, fibroblast, Cockayne syndrome) - GEIMM
IGF075/76 (skin, fibroblast) - GEIMM
IGF075/77 (skin, fibroblast) - GEIMM
IGF075/78 (skin, fibroblast, aspartylglycosaminuria) - GEIMM
IGF075/80 (skin, fibroblast, sulfatidosis, juvenile, Austin type) - GEIMM
IGF075/81 (skin, fibroblast, Krabbe disease) - GEIMM
IGF075/82 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF075/84 (skin, fibroblast) - GEIMM
IGF075/86 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF075/87 (skin, fibroblast) - GEIMM
IGF075/88 (skin, fibroblast) - GEIMM
IGF075/89 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF075/90 (skin, fibroblast) - GEIMM
IGF075/91 (skin, fibroblast) - GEIMM
IGF075/95 (skin, fibroblast) - GEIMM
IGF076/76 (skin, fibroblast) - GEIMM
IGF076/78 (skin, fibroblast) - GEIMM
IGF076/79 (skin, fibroblast) - GEIMM
IGF076/81 (skin, fibroblast) - GEIMM
IGF076/82 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF076/83 (skin, fibroblast) - GEIMM
IGF076/84 (skin, fibroblast, dystonia musculorum deformans 2) - GEIMM
IGF076/85 (skin, fibroblast) - GEIMM
IGF076/87 (skin, fibroblast) - GEIMM
IGF076/89 (skin, fibroblast, Smith-McCort dwarfism) - GEIMM
IGF076/90 (skin, fibroblast) - GEIMM
IGF076/91 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF076/92 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF076/95 (skin, fibroblast) - GEIMM
IGF077/76 (skin, fibroblast) - GEIMM
IGF077/77 (skin, fibroblast) - GEIMM
IGF077/78 (skin, fibroblast) - GEIMM
IGF077/79 (skin, fibroblast) - GEIMM
IGF077/80 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF077/81 (skin, fibroblast, Krabbe disease) - GEIMM
IGF077/83 (skin, fibroblast) - GEIMM
IGF077/84 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF077/85 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF077/86 (skin, fibroblast) - GEIMM
IGF077/87 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF077/88 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF077/89 (skin, fibroblast, mucolipidosis III) - GEIMM
IGF077/91 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF077/92 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF077/95 (skin, fibroblast) - GEIMM
IGF078/78 (skin, fibroblast) - GEIMM
IGF078/79 (skin, fibroblast) - GEIMM
IGF078/80 (skin, fibroblast) - GEIMM
IGF078/81 (skin, fibroblast) - GEIMM
IGF078/83 (skin, fibroblast) - GEIMM
IGF078/84 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF078/85 (skin, fibroblast) - GEIMM
IGF078/86 (skin, fibroblast) - GEIMM
IGF078/87 (skin, fibroblast) - GEIMM
IGF078/89 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF078/90 (skin, fibroblast) - GEIMM
IGF078/91 (skin, fibroblast) - GEIMM
IGF078/92 (skin, fibroblast) - GEIMM
IGF078/95 (skin, fibroblast) - GEIMM
IGF079/76 (skin, fibroblast, Ehlers-Danlos syndrome) - GEIMM
IGF079/77 (skin, fibroblast) - GEIMM
IGF079/78 (skin, fibroblast, spondyloepiphyseal dysplasia, congenital) - GEIMM
IGF079/80 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF079/81 (skin, fibroblast) - GEIMM
IGF079/82 (skin, fibroblast) - GEIMM
IGF079/83 (skin, fibroblast) - GEIMM
IGF079/84 (skin, fibroblast) - GEIMM
IGF079/86 (skin, fibroblast) - GEIMM
IGF079/87 (skin, fibroblast) - GEIMM
IGF079/89 (skin, fibroblast, familial dolichocephaly) - GEIMM
IGF079/90 (skin, fibroblast, early myoclonic encephalopathy) - GEIMM
IGF079/91 (skin, fibroblast) - GEIMM
IGF080/76 (skin, fibroblast, mucolipidosis III) - GEIMM
IGF080/78 (skin, fibroblast) - GEIMM
IGF080/80 (skin, fibroblast) - GEIMM
IGF080/81 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF080/82 (skin, fibroblast) - GEIMM
IGF080/83 (skin, fibroblast) - GEIMM
IGF080/84 (skin, fibroblast) - GEIMM
IGF080/85 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF080/86 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF080/87 (skin, fibroblast) - GEIMM
IGF080/89 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF080/90 (skin, fibroblast) - GEIMM
IGF080/91 (skin, fibroblast) - GEIMM
IGF081/76 (skin, fibroblast, mucolipidosis III) - GEIMM
IGF081/78 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - GEIMM
IGF081/80 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF081/81 (skin, fibroblast, Menkes syndrome) - GEIMM
IGF081/82 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF081/83 (skin, fibroblast) - GEIMM
IGF081/84 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF081/86 (skin, fibroblast, diastrophic dysplasia) - GEIMM
IGF081/87 (skin, fibroblast) - GEIMM
IGF081/89 (skin, fibroblast, sudden infant death syndrome) - GEIMM
IGF081/90 (skin, fibroblast, fucosidosis) - GEIMM
IGF081/91 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF081/92 (skin, fibroblast, Sjogren-Larsson syndrome) - GEIMM
IGF082/76 (skin, fibroblast, Farber lipogranulomatosis) - GEIMM
IGF082/80 (skin, fibroblast) - GEIMM
IGF082/81 (skin, fibroblast) - GEIMM
IGF082/82 (skin, fibroblast) - GEIMM
IGF082/83 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF082/84 (skin, fibroblast) - GEIMM
IGF082/85 (skin, fibroblast) - GEIMM
IGF082/86 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF082/87 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF082/89 (skin, fibroblast) - GEIMM
IGF082/90 (skin, fibroblast) - GEIMM
IGF082/91 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF082/92 (skin, fibroblast) - GEIMM
IGF083/76 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF083/78 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF083/80 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF083/81 (skin, fibroblast) - GEIMM
IGF083/82 (skin, fibroblast, hyperglycinemia, nonketotic) - GEIMM
IGF083/83 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF083/84 (skin, fibroblast, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF083/85 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF083/86 (skin, fibroblast) - GEIMM
IGF083/87 (skin, fibroblast) - GEIMM
IGF083/89 (skin, fibroblast) - GEIMM
IGF083/90 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF083/91 (skin, fibroblast) - GEIMM
IGF083/92 (skin, fibroblast) - GEIMM
IGF084/80 (skin, fibroblast) - GEIMM
IGF084/81 (skin, fibroblast) - GEIMM
IGF084/82 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF084/83 (skin, fibroblast) - GEIMM
IGF084/84 (skin, fibroblast) - GEIMM
IGF084/85 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF084/86 (skin, fibroblast) - GEIMM
IGF084/89 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF084/90 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF084/91 (skin, fibroblast, proteolipid protein, myelin) - GEIMM
IGF084/92 (skin, fibroblast) - GEIMM
IGF085/78 (skin, fibroblast) - GEIMM
IGF085/80 (skin, fibroblast) - GEIMM
IGF085/82 (skin, fibroblast) - GEIMM
IGF085/84 (skin, fibroblast) - GEIMM
IGF085/85 (skin, fibroblast) - GEIMM
IGF085/86 (skin, fibroblast, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF085/89 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF085/90 (skin, fibroblast, Krabbe disease) - GEIMM
IGF085/91 (skin, fibroblast) - GEIMM
IGF085/92 (skin, fibroblast) - GEIMM
IGF086/78 (skin, fibroblast, Krabbe disease) - GEIMM
IGF086/79 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF086/80 (skin, fibroblast) - GEIMM
IGF086/84 (skin, fibroblast) - GEIMM
IGF086/85 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF086/86 (skin, fibroblast) - GEIMM
IGF086/89 (skin, fibroblast) - GEIMM
IGF086/90 (skin, fibroblast, Lesch-Nyhan syndrome) - GEIMM
IGF086/91 (skin, fibroblast, adrenoleukodystrophy / addison disease and cerebral sclerosis) - GEIMM
IGF086/92 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF087/78 (skin, fibroblast) - GEIMM
IGF087/79 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF087/80 (skin, fibroblast) - GEIMM
IGF087/81 (skin, fibroblast) - GEIMM
IGF087/82 (skin, fibroblast) - GEIMM
IGF087/83 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF087/84 (skin, fibroblast) - GEIMM
IGF087/85 (skin, fibroblast) - GEIMM
IGF087/86 (skin, fibroblast) - GEIMM
IGF087/87 (skin, fibroblast) - GEIMM
IGF087/89 (skin, fibroblast) - GEIMM
IGF087/91 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF087/92 (skin, fibroblast, spongy degeneration of central nervous system /Canavan disease) - GEIMM
IGF088/78 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF088/79 (skin, fibroblast) - GEIMM
IGF088/82 (skin, fibroblast) - GEIMM
IGF088/83 (skin, fibroblast) - GEIMM
IGF088/84 (skin, fibroblast) - GEIMM
IGF088/86 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF088/87 (skin, fibroblast) - GEIMM
IGF088/89 (skin, fibroblast) - GEIMM
IGF088/90 (skin, fibroblast) - GEIMM
IGF088/91 (skin, fibroblast) - GEIMM
IGF088/92 (skin, fibroblast) - GEIMM
IGF089/78 (skin, fibroblast) - GEIMM
IGF089/79 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF089/80 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF089/81 (skin, fibroblast) - GEIMM
IGF089/82 (skin, fibroblast, frontometaphyseal dysplasia) - GEIMM
IGF089/83 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF089/84 (skin, fibroblast) - GEIMM
IGF089/85 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF089/87 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF089/89 (skin, fibroblast, osteogenesis imperfecta, type II) - GEIMM
IGF089/90 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF089/91 (skin, fibroblast) - GEIMM
IGF089/92 (skin, fibroblast) - GEIMM
IGF090/78 (skin, fibroblast, Laurence-Moon syndrome) - GEIMM
IGF090/79 (skin, fibroblast) - GEIMM
IGF090/82 (skin, fibroblast) - GEIMM
IGF090/83 (skin, fibroblast) - GEIMM
IGF090/84 (skin, fibroblast) - GEIMM
IGF090/86 (skin, fibroblast, Larsen syndrome) - GEIMM
IGF090/87 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF090/89 (skin, fibroblast) - GEIMM
IGF090/91 (skin, fibroblast, carboydrate deficient glycoprotein syndrome, type I) - GEIMM
IGF090/92 (skin, fibroblast) - GEIMM
IGF091/78 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF091/79 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF091/81 (skin, fibroblast) - GEIMM
IGF091/82 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF091/83 (skin, fibroblast) - GEIMM
IGF091/84 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF091/85 (skin, fibroblast, argininosuccinicaciduria) - GEIMM
IGF091/86 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF091/87 (skin, fibroblast) - GEIMM
IGF091/89 (skin, fibroblast) - GEIMM
IGF091/92 (skin, fibroblast) - GEIMM
IGF092/78 (skin, fibroblast) - GEIMM
IGF092/82 (skin, fibroblast, phenylketonuria I) - GEIMM
IGF092/83 (skin, fibroblast) - GEIMM
IGF092/84 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF092/86 (skin, fibroblast) - GEIMM
IGF092/87 (skin, fibroblast) - GEIMM
IGF093/78 (skin, fibroblast) - GEIMM
IGF093/80 (skin, fibroblast) - GEIMM
IGF093/81 (skin, fibroblast) - GEIMM
IGF093/82 (skin, fibroblast) - GEIMM
IGF093/83 (skin, fibroblast) - GEIMM
IGF093/84 (skin, fibroblast) - GEIMM
IGF093/85 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF093/86 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF093/87 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF093/89 (skin, fibroblast, osteogenesis imperfecta, type IV) - GEIMM
IGF093/90 (skin, fibroblast) - GEIMM
IGF093/91 (skin, fibroblast, Krabbe disease) - GEIMM
IGF093/92 (skin, fibroblast) - GEIMM
IGF094/78 (skin, fibroblast, arsa pseudodeficiency) - GEIMM
IGF094/80 (skin, fibroblast) - GEIMM
IGF094/81 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF094/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF094/84 (skin, fibroblast) - GEIMM
IGF094/85 (skin, fibroblast) - GEIMM
IGF094/86 (skin, fibroblast) - GEIMM
IGF094/87 (skin, fibroblast) - GEIMM
IGF094/89 (skin, fibroblast) - GEIMM
IGF094/90 (skin, fibroblast) - GEIMM
IGF094/91 (skin, fibroblast) - GEIMM
IGF094/92 (skin, fibroblast, homocystinuria - megaloblastic anemia) - GEIMM
IGF095/78 (skin, fibroblast) - GEIMM
IGF095/79 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF095/80 (skin, fibroblast) - GEIMM
IGF095/82 (skin, fibroblast) - GEIMM
IGF095/83 (skin, fibroblast) - GEIMM
IGF095/85 (skin, fibroblast, Shwachman-Bodian syndrome) - GEIMM
IGF095/86 (skin, fibroblast, Krabbe disease) - GEIMM
IGF095/87 (skin, fibroblast) - GEIMM
IGF095/89 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF095/91 (skin, fibroblast) - GEIMM
IGF096/78 (skin, fibroblast) - GEIMM
IGF096/79 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF096/80 (skin, fibroblast) - GEIMM
IGF096/81 (skin, fibroblast) - GEIMM
IGF096/82 (skin, fibroblast, Ehlers-Danlos syndrome) - GEIMM
IGF096/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF096/84 (skin, fibroblast, camptomelic dwarfism) - GEIMM
IGF096/85 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF096/86 (skin, fibroblast) - GEIMM
IGF096/90 (skin, fibroblast) - GEIMM
IGF096/91 (skin, fibroblast) - GEIMM
IGF096/92 (skin, fibroblast) - GEIMM
IGF097/78 (skin, fibroblast) - GEIMM
IGF097/79 (skin, fibroblast) - GEIMM
IGF097/80 (skin, fibroblast) - GEIMM
IGF097/81 (skin, fibroblast) - GEIMM
IGF097/82 (skin, fibroblast) - GEIMM
IGF097/83 (skin, fibroblast) - GEIMM
IGF097/84 (skin, fibroblast) - GEIMM
IGF097/85 (skin, fibroblast) - GEIMM
IGF097/86 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF097/87 (skin, fibroblast) - GEIMM
IGF097/89 (skin, fibroblast, cri du chat syndrome) - GEIMM
IGF097/90 (skin, fibroblast, spastic paraparesis) - GEIMM
IGF097/92 (skin, fibroblast) - GEIMM
IGF098/78 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF098/79 (skin, fibroblast) - GEIMM
IGF098/80 (skin, fibroblast) - GEIMM
IGF098/82 (skin, fibroblast) - GEIMM
IGF098/83 (skin, fibroblast) - GEIMM
IGF098/84 (skin, fibroblast) - GEIMM
IGF098/85 (skin, fibroblast) - GEIMM
IGF098/86 (skin, fibroblast, osteogenesis imperfecta type I (with opalescent teeth)) - GEIMM
IGF098/87 (skin, fibroblast) - GEIMM
IGF098/89 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF098/90 (skin, fibroblast) - GEIMM
IGF098/92 (skin, fibroblast, glyceronephosphate o-acyltransferase) - GEIMM
IGF099/78 (skin, fibroblast) - GEIMM
IGF099/79 (skin, fibroblast, adrenal hyperplasia III) - GEIMM
IGF099/80 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF099/82 (skin, fibroblast) - GEIMM
IGF099/83 (skin, fibroblast) - GEIMM
IGF099/84 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF099/85 (skin, fibroblast) - GEIMM
IGF099/86 (skin, fibroblast, fibrodysplasia ossificans progressiva) - GEIMM
IGF099/87 (skin, fibroblast) - GEIMM
IGF099/89 (skin, fibroblast) - GEIMM
IGF099/90 (skin, fibroblast, spinal muscolar atrophy III) - GEIMM
IGF099/92 (skin, fibroblast) - GEIMM
IGF100/78 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF100/79 (skin, fibroblast) - GEIMM
IGF100/80 (skin, fibroblast) - GEIMM
IGF100/81 (skin, fibroblast, porphiria, acute intermittent) - GEIMM
IGF100/83 (skin, fibroblast) - GEIMM
IGF100/84 (skin, fibroblast) - GEIMM
IGF100/85 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF100/86 (skin, fibroblast) - GEIMM
IGF100/87 (skin, fibroblast) - GEIMM
IGF100/89 (skin, fibroblast, spinal muscolar atrophy I / Werdnig-Hoffmann disease) - GEIMM
IGF100/90 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF100/91 (skin, fibroblast, articular hypermobility syndrome) - GEIMM
IGF100/92 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF101/78 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF101/79 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF101/80 (skin, fibroblast, homocystinuria) - GEIMM
IGF101/81 (skin, fibroblast, trichothiodystrophy) - GEIMM
IGF101/82 (skin, fibroblast) - GEIMM
IGF101/83 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF101/84 (skin, fibroblast) - GEIMM
IGF101/85 (skin, fibroblast) - GEIMM
IGF101/86 (skin, fibroblast) - GEIMM
IGF101/89 (skin, fibroblast) - GEIMM
IGF101/90 (skin, fibroblast) - GEIMM
IGF101/91 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF102/78 (skin, fibroblast, neuraminidase deficiency) - GEIMM
IGF102/80 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF102/82 (skin, fibroblast) - GEIMM
IGF102/83 (skin, fibroblast, hyperlipoproteinemia I) - GEIMM
IGF102/84 (skin, fibroblast) - GEIMM
IGF102/85 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF102/86 (skin, fibroblast) - GEIMM
IGF102/87 (skin, fibroblast) - GEIMM
IGF102/89 (skin, fibroblast, trisomy 21 / Down syndrome) - GEIMM
IGF102/90 (skin, fibroblast) - GEIMM
IGF102/91 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF103/79 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF103/81 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF103/82 (skin, fibroblast) - GEIMM
IGF103/84 (skin, fibroblast) - GEIMM
IGF103/85 (skin, fibroblast) - GEIMM
IGF103/86 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF103/89 (skin, fibroblast) - GEIMM
IGF103/90 (skin, fibroblast) - GEIMM
IGF103/91 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF104/78 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF104/79 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF104/81 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF104/82 (skin, fibroblast, Lesch-Nyhan syndrome) - GEIMM
IGF104/83 (skin, fibroblast) - GEIMM
IGF104/84 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF104/85 (skin, fibroblast) - GEIMM
IGF104/89 (skin, fibroblast) - GEIMM
IGF104/90 (skin, fibroblast) - GEIMM
IGF104/91 (skin, fibroblast) - GEIMM
IGF105/80 (skin, fibroblast) - GEIMM
IGF105/81 (skin, fibroblast, fucosidosis) - GEIMM
IGF105/82 (skin, fibroblast) - GEIMM
IGF105/83 (skin, fibroblast) - GEIMM
IGF105/84 (skin, fibroblast) - GEIMM
IGF105/85 (skin, fibroblast, Lowe oculocerebrorenal syndrome) - GEIMM
IGF105/87 (skin, fibroblast) - GEIMM
IGF105/89 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGF105/91 (skin, fibroblast) - GEIMM
IGF106/78 (skin, fibroblast) - GEIMM
IGF106/79 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF106/80 (skin, fibroblast) - GEIMM
IGF106/81 (skin, fibroblast) - GEIMM
IGF106/82 (skin, fibroblast) - GEIMM
IGF106/83 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF106/84 (skin, fibroblast) - GEIMM
IGF106/85 (skin, fibroblast) - GEIMM
IGF106/90 (skin, fibroblast) - GEIMM
IGF106/91 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF107/80 (skin, fibroblast) - GEIMM
IGF107/81 (skin, fibroblast, fructose intolerance, hereditary) - GEIMM
IGF107/82 (skin, fibroblast, Bardet-Biedl syndrome) - GEIMM
IGF107/83 (skin, fibroblast) - GEIMM
IGF107/84 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF107/85 (skin, fibroblast) - GEIMM
IGF107/89 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF107/90 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF107/91 (skin, fibroblast) - GEIMM
IGF108/80 (skin, fibroblast) - GEIMM
IGF108/81 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF108/82 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF108/83 (skin, fibroblast, hyperammonemia due to carbamoylphosphate synthetase deficien.) - GEIMM
IGF108/84 (skin, fibroblast) - GEIMM
IGF108/85 (skin, fibroblast) - GEIMM
IGF108/90 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF108/91 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF109/79 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF109/80 (skin, fibroblast) - GEIMM
IGF109/81 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF109/83 (skin, fibroblast) - GEIMM
IGF109/84 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF109/85 (skin, fibroblast, Laurence-Moon syndrome) - GEIMM
IGF109/91 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - GEIMM
IGF110/78 (skin, fibroblast, homocystinuria) - GEIMM
IGF110/80 (skin, fibroblast) - GEIMM
IGF110/81 (skin, fibroblast) - GEIMM
IGF110/82 (skin, fibroblast, glycogen storage disease I) - GEIMM
IGF110/83 (skin, fibroblast) - GEIMM
IGF110/85 (skin, fibroblast, complex IV,mitocondrial respiratory chain,deficiency of) - GEIMM
IGF110/91 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF111/80 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF111/82 (skin, fibroblast) - GEIMM
IGF111/83 (skin, fibroblast, galactose epimerase deficiency) - GEIMM
IGF111/84 (skin, fibroblast) - GEIMM
IGF111/85 (skin, fibroblast) - GEIMM
IGF111/90 (skin, fibroblast) - GEIMM
IGF112/80 (skin, fibroblast) - GEIMM
IGF112/81 (skin, fibroblast) - GEIMM
IGF112/82 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF112/83 (skin, fibroblast) - GEIMM
IGF112/84 (skin, fibroblast) - GEIMM
IGF112/85 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF112/87 (skin, fibroblast) - GEIMM
IGF112/91 (skin, fibroblast) - GEIMM
IGF113/80 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF113/81 (skin, fibroblast, methylmalonicacidemia) - GEIMM
IGF113/82 (skin, fibroblast) - GEIMM
IGF113/83 (skin, fibroblast, Berardinelli syndrome /seip syndrome) - GEIMM
IGF113/84 (skin, fibroblast) - GEIMM
IGF113/85 (skin, fibroblast, Marfan syndrome) - GEIMM
IGF113/87 (skin, fibroblast) - GEIMM
IGF113/91 (skin, fibroblast, mucopolysaccharidosis type III B) - GEIMM
IGF114/82 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF114/83 (skin, fibroblast) - GEIMM
IGF114/84 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF114/85 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF114/87 (skin, fibroblast) - GEIMM
IGF114/91 (skin, fibroblast) - GEIMM
IGF115/81 (skin, fibroblast) - GEIMM
IGF115/82 (skin, fibroblast) - GEIMM
IGF115/83 (skin, fibroblast) - GEIMM
IGF115/84 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF115/85 (skin, fibroblast) - GEIMM
IGF115/90 (skin, fibroblast, leprechaunism) - GEIMM
IGF115/91 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF116/81 (skin, fibroblast) - GEIMM
IGF116/82 (skin, fibroblast, Gaucher disease type II) - GEIMM
IGF116/83 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF116/84 (skin, fibroblast) - GEIMM
IGF116/85 (skin, fibroblast) - GEIMM
IGF116/91 (skin, fibroblast) - GEIMM
IGF117/80 (skin, fibroblast) - GEIMM
IGF117/81 (skin, fibroblast) - GEIMM
IGF117/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF117/84 (skin, fibroblast, fibrodysplasia ossificans progressiva) - GEIMM
IGF117/85 (skin, fibroblast, amaurotic family idiocy, late infantile type/NCL late infantile) - GEIMM
IGF117/91 (skin, fibroblast, osteogenesis imperfecta) - GEIMM
IGF118/80 (skin, fibroblast, glycogen storage disease II) - GEIMM
IGF118/81 (skin, fibroblast, mucolipidosis II) - GEIMM
IGF118/82 (skin, fibroblast) - GEIMM
IGF118/84 (skin, fibroblast) - GEIMM
IGF118/85 (skin, fibroblast) - GEIMM
IGF118/91 (skin, fibroblast, mucopolysaccharidosis type II) - GEIMM
IGF119/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF119/84 (skin, fibroblast) - GEIMM
IGF119/85 (skin, fibroblast) - GEIMM
IGF119/91 (skin, fibroblast) - GEIMM
IGF120/81 (skin, fibroblast, maple syrup urine disease) - GEIMM
IGF120/82 (skin, fibroblast) - GEIMM
IGF120/83 (skin, fibroblast, triglyceride storage disease) - GEIMM
IGF120/84 (skin, fibroblast, fucosidosis) - GEIMM
IGF120/85 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF120/91 (skin, fibroblast) - GEIMM
IGF121/80 (skin, fibroblast) - GEIMM
IGF121/82 (skin, fibroblast) - GEIMM
IGF121/83 (skin, fibroblast) - GEIMM
IGF121/84 (skin, fibroblast) - GEIMM
IGF121/85 (skin, fibroblast) - GEIMM
IGF121/91 (skin, fibroblast, mucopolysaccharidosis type III C) - GEIMM
IGF122/82 (skin, fibroblast) - GEIMM
IGF122/83 (skin, fibroblast) - GEIMM
IGF122/84 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - GEIMM
IGF122/85 (skin, fibroblast) - GEIMM
IGF122/91 (skin, fibroblast, pyruvate dehydrogenase def.) - GEIMM
IGF123/80 (skin, fibroblast) - GEIMM
IGF123/81 (skin, fibroblast) - GEIMM
IGF123/82 (skin, fibroblast) - GEIMM
IGF123/83 (skin, fibroblast) - GEIMM
IGF123/84 (skin, fibroblast) - GEIMM
IGF123/85 (skin, fibroblast) - GEIMM
IGF123/91 (skin, fibroblast, Krabbe disease) - GEIMM
IGF124/80 (skin, fibroblast) - GEIMM
IGF124/81 (skin, fibroblast, xeroderma pigmentosum I) - GEIMM
IGF124/82 (skin, fibroblast, Jarcho-Levin syndrome) - GEIMM
IGF124/84 (skin, fibroblast, Sandhoff disease) - GEIMM
IGF124/85 (skin, fibroblast) - GEIMM
IGF124/91 (skin, fibroblast) - GEIMM
IGF125/80 (skin, fibroblast) - GEIMM
IGF125/81 (skin, fibroblast, xeroderma pigmentosum I) - GEIMM
IGF125/82 (skin, fibroblast, dibasicaminoaciduria II) - GEIMM
IGF125/84 (skin, fibroblast, fibrodysplasia ossificans progressiva) - GEIMM
IGF125/85 (skin, fibroblast) - GEIMM
IGF126/80 (skin, fibroblast) - GEIMM
IGF126/81 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF126/83 (skin, fibroblast) - GEIMM
IGF126/84 (skin, fibroblast) - GEIMM
IGF126/85 (skin, fibroblast) - GEIMM
IGF126/91 (skin, fibroblast, congenital undergrowth of left leg) - GEIMM
IGF127/80 (skin, fibroblast) - GEIMM
IGF127/82 (skin, fibroblast, Alexander disease) - GEIMM
IGF127/83 (skin, fibroblast) - GEIMM
IGF127/85 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF127/91 (skin, fibroblast, Tay-Sachs disease) - GEIMM
IGF128/80 (skin, fibroblast) - GEIMM
IGF128/83 (skin, fibroblast) - GEIMM
IGF128/84 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF128/85 (skin, fibroblast) - GEIMM
IGF128/91 (skin, fibroblast, adrenal gland tumor) - GEIMM
IGF129/80 (skin, fibroblast, mucopolysaccharidosis type VI) - GEIMM
IGF129/82 (skin, fibroblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGF129/84 (skin, fibroblast) - GEIMM
IGF130/82 (skin, fibroblast, tyrosine transaminase deficiency) - GEIMM
IGF130/83 (skin, fibroblast, Lesch-Nyhan syndrome) - GEIMM
IGF130/84 (skin, fibroblast) - GEIMM
IGF130/91 (skin, fibroblast, B1 variant - GM2 gangliosidosis / Tay-Sachs disease) - GEIMM
IGF131/80 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF131/82 (skin, fibroblast) - GEIMM
IGF131/83 (skin, fibroblast, dystonia musculorum deformans 2) - GEIMM
IGF131/84 (skin, fibroblast) - GEIMM
IGF132/80 (skin, fibroblast, Charcot-Marie-Tooth disease) - GEIMM
IGF132/82 (skin, fibroblast) - GEIMM
IGF132/83 (skin, fibroblast) - GEIMM
IGF133/80 (skin, fibroblast) - GEIMM
IGF133/82 (skin, fibroblast) - GEIMM
IGF133/83 (skin, fibroblast) - GEIMM
IGF134/82 (skin, fibroblast, fucosidosis) - GEIMM
IGF134/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF135/80 (skin, fibroblast) - GEIMM
IGF135/82 (skin, fibroblast, spongy degeneration of central nervous system /Canavan disease) - GEIMM
IGF135/83 (skin, fibroblast, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF136/80 (skin, fibroblast) - GEIMM
IGF136/82 (skin, fibroblast) - GEIMM
IGF136/83 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF137/80 (skin, fibroblast, Charcot-Marie-Tooth disease) - GEIMM
IGF137/83 (skin, fibroblast, angiokeratoma, diffuse / Fabry disease) - GEIMM
IGF138/80 (skin, fibroblast) - GEIMM
IGF138/82 (skin, fibroblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGF138/83 (skin, fibroblast) - GEIMM
IGF139/80 (skin, fibroblast, Charcot-Marie-Tooth disease) - GEIMM
IGF139/83 (skin, fibroblast) - GEIMM
IGF140/80 (skin, fibroblast) - GEIMM
IGF140/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF141/80 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF141/82 (skin, fibroblast, xerodermic idiocy of De Sanctis and Cacchione) - GEIMM
IGF141/83 (skin, fibroblast, trisomy 21 / Down syndrome) - GEIMM
IGF142/80 (skin, fibroblast, Gaucher disease type I) - GEIMM
IGF142/83 (skin, fibroblast) - GEIMM
IGF143/80 (skin, fibroblast) - GEIMM
IGF143/82 (skin, fibroblast, phenylketonuria I) - GEIMM
IGF143/83 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGF144/80 (skin, fibroblast, cystic fibrosis) - GEIMM
IGF144/82 (skin, fibroblast, phenylketonuria I) - GEIMM
IGF144/83 (skin, fibroblast) - GEIMM
IGF145/80 (skin, fibroblast) - GEIMM
IGF145/83 (skin, fibroblast) - GEIMM
IGF146/80 (skin, fibroblast, ornithine-transcarbamylase deficiency) - GEIMM
IGF146/82 (skin, fibroblast, sialic acid storage disease) - GEIMM
IGF147/82 (skin, fibroblast) - GEIMM
IGF147/83 (skin, fibroblast) - GEIMM
IGF148/82 (skin, fibroblast) - GEIMM
IGF148/83 (skin, fibroblast) - GEIMM
IGF149/82 (skin, fibroblast) - GEIMM
IGF149/83 (skin, fibroblast, mucopolysaccharidosis type IV B / Morquio syndrome) - GEIMM
IGF150/83 (skin, fibroblast) - GEIMM
IGF151/82 (skin, fibroblast) - GEIMM
IGF151/83 (skin, fibroblast) - GEIMM
IGF152/82 (skin, fibroblast) - GEIMM
IGF152/83 (skin, fibroblast, Niemann-Pick disease, type A) - GEIMM
IGF153/82 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF153/83 (skin, fibroblast) - GEIMM
IGF154/82 (skin, fibroblast) - GEIMM
IGF154/83 (skin, fibroblast, glycogen storage disease III) - GEIMM
IGF155/82 (skin, fibroblast) - GEIMM
IGF156/82 (skin, fibroblast, xerodermic idiocy of De Sanctis and Cacchione) - GEIMM
IGF156/83 (skin, fibroblast) - GEIMM
IGF157/82 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF157/83 (skin, fibroblast) - GEIMM
IGF158/82 (skin, fibroblast, sponastrime dysplasia) - GEIMM
IGF158/83 (skin, fibroblast) - GEIMM
IGF159/82 (skin, fibroblast) - GEIMM
IGF159/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF160/82 (skin, fibroblast, Niemann-Pick disease, type B) - GEIMM
IGF160/83 (skin, fibroblast, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGF161/83 (skin, fibroblast, propionicacidemia I) - GEIMM
IGF162/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF163/83 (skin, fibroblast, Gaucher disease type III) - GEIMM
IGF164/83 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - GEIMM
IGF165/83 (skin, fibroblast) - GEIMM
IGF166/83 (skin, fibroblast, trichothiodystrophy) - GEIMM
IGF168/83 (skin, fibroblast) - GEIMM
IGF169/83 (skin, fibroblast, mucopolysaccharidosis type III A) - GEIMM
IGF170/83 (skin, fibroblast) - GEIMM
IGF171/83 (skin, fibroblast) - GEIMM
IGF172/83 (skin, fibroblast) - GEIMM
IGF173/83 (skin, fibroblast) - GEIMM
IGF174/83 (skin, fibroblast) - GEIMM
IGF175/83 (skin, fibroblast) - GEIMM
IGF176/83 (skin, fibroblast) - GEIMM
IGF177/83 (skin, fibroblast) - GEIMM
IGF178/83 (skin, fibroblast) - GEIMM
IGF179/83 (skin, fibroblast) - GEIMM
IGF180/83 (skin, fibroblast, Niemann-Pick disease, type C) - GEIMM
IGF181/83 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - GEIMM
IGF182/83 (skin, fibroblast, gangliosidosis, generalized GM1, type II) - GEIMM
IGF183/83 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - GEIMM
IGF186/83 (skin, fibroblast) - GEIMM
IGF187/83 (skin, fibroblast, hyperglycinemia, nonketotic) - GEIMM
IGF200/83 (skin, fibroblast) - GEIMM
IGF201/83 (skin, fibroblast) - GEIMM
IGF740/88 (skin, fibroblast, mucopolysaccharidosis type IV A) - GEIMM
IGL001/01 (lymphoblast) - GEIMM
IGL001/91 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL001/92 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL001/93 (lymphoblast, fucosidosis) - GEIMM
IGL001/95 (lymphoblast) - GEIMM
IGL001/96 (lymphoblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGL001/97 (lymphoblast) - GEIMM
IGL001/98 (lymphoblast) - GEIMM
IGL001/99 (lymphoblast) - GEIMM
IGL002/00 (lymphoblast) - GEIMM
IGL002/01 (lymphoblast) - GEIMM
IGL002/91 (lymphoblast) - GEIMM
IGL002/92 (lymphoblast, Aicardi syndrome / corpus callosum) - GEIMM
IGL002/93 (lymphoblast, fucosidosis) - GEIMM
IGL002/94 (lymphoblast) - GEIMM
IGL002/96 (lymphoblast) - GEIMM
IGL002/98 (lymphoblast) - GEIMM
IGL002/99 (lymphoblast) - GEIMM
IGL003/00 (lymphoblast) - GEIMM
IGL003/01 (lymphoblast) - GEIMM
IGL003/91 (lymphoblast) - GEIMM
IGL003/92 (lymphoblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGL003/93 (lymphoblast) - GEIMM
IGL003/95 (lymphoblast, glycogen storage disease II) - GEIMM
IGL003/96 (lymphoblast, Berardinelli syndrome /seip syndrome) - GEIMM
IGL003/97 (lymphoblast) - GEIMM
IGL003/98 (lymphoblast) - GEIMM
IGL003/99 (lymphoblast, methylenetetra-hydrofolate reductase def.) - GEIMM
IGL004/00 (lymphoblast) - GEIMM
IGL004/01 (lymphoblast) - GEIMM
IGL004/91 (lymphoblast) - GEIMM
IGL004/93 (lymphoblast) - GEIMM
IGL004/94 (lymphoblast, autoimmune polyendocrinopathy syndrome,type I) - GEIMM
IGL004/96 (lymphoblast) - GEIMM
IGL004/97 (lymphoblast) - GEIMM
IGL004/98 (lymphoblast) - GEIMM
IGL004/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL005/00 (lymphoblast) - GEIMM
IGL005/01 (lymphoblast) - GEIMM
IGL005/91 (lymphoblast, mucopolysaccharidosis type III B) - GEIMM
IGL005/92 (lymphoblast, articular hypermobility syndrome) - GEIMM
IGL005/93 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL005/95 (lymphoblast) - GEIMM
IGL005/97 (lymphoblast) - GEIMM
IGL005/98 (lymphoblast, Niemann-Pick disease, type A) - GEIMM
IGL005/99 (lymphoblast) - GEIMM
IGL006/00 (lymphoblast) - GEIMM
IGL006/01 (lymphoblast) - GEIMM
IGL006/92 (lymphoblast) - GEIMM
IGL006/93 (lymphoblast) - GEIMM
IGL006/95 (lymphoblast) - GEIMM
IGL006/97 (lymphoblast) - GEIMM
IGL006/98 (lymphoblast, glycogen storage disease II) - GEIMM
IGL006/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL007/00 (lymphoblast) - GEIMM
IGL007/01 (lymphoblast) - GEIMM
IGL007/91 (lymphoblast, Krabbe disease) - GEIMM
IGL007/92 (lymphoblast) - GEIMM
IGL007/94 (lymphoblast, Gaucher disease type I) - GEIMM
IGL007/96 (lymphoblast) - GEIMM
IGL007/98 (lymphoblast, Gaucher disease type I) - GEIMM
IGL007/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL008/00 (lymphoblast, salla disease) - GEIMM
IGL008/92 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL008/93 (lymphoblast, Alagille syndrome) - GEIMM
IGL008/94 (lymphoblast, metachromatic leukodystrophy, late-infantile) - GEIMM
IGL008/96 (lymphoblast) - GEIMM
IGL008/98 (lymphoblast) - GEIMM
IGL008/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL009/00 (lymphoblast) - GEIMM
IGL009/01 (lymphoblast) - GEIMM
IGL009/92 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL009/96 (lymphoblast, acyl-CoA dehydrogenase, long-chain, deficiency) - GEIMM
IGL009/97 (lymphoblast) - GEIMM
IGL009/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL010/00 (lymphoblast) - GEIMM
IGL010/92 (lymphoblast) - GEIMM
IGL010/94 (lymphoblast) - GEIMM
IGL010/98 (lymphoblast) - GEIMM
IGL010/99 (lymphoblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGL011/00 (lymphoblast) - GEIMM
IGL011/01 (lymphoblast) - GEIMM
IGL011/96 (lymphoblast) - GEIMM
IGL011/97 (lymphoblast) - GEIMM
IGL011/98 (lymphoblast, Gaucher disease type I) - GEIMM
IGL011/99 (lymphoblast, mucopolysaccharidosis type III A) - GEIMM
IGL012/00 (lymphoblast) - GEIMM
IGL012/01 (lymphoblast) - GEIMM
IGL012/95 (lymphoblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGL012/97 (lymphoblast) - GEIMM
IGL012/98 (lymphoblast) - GEIMM
IGL012/99 (lymphoblast) - GEIMM
IGL013/00 (lymphoblast) - GEIMM
IGL013/01 (lymphoblast) - GEIMM
IGL013/95 (lymphoblast) - GEIMM
IGL013/96 (lymphoblast) - GEIMM
IGL013/97 (lymphoblast) - GEIMM
IGL013/98 (lymphoblast, mucopolysaccharidosis type III C) - GEIMM
IGL013/99 (lymphoblast) - GEIMM
IGL014/00 (lymphoblast, Gaucher disease type I) - GEIMM
IGL014/01 (lymphoblast) - GEIMM
IGL014/95 (lymphoblast) - GEIMM
IGL014/96 (lymphoblast) - GEIMM
IGL014/97 (lymphoblast) - GEIMM
IGL014/98 (lymphoblast, Niemann-Pick disease, type A) - GEIMM
IGL014/99 (lymphoblast, mucopolysaccharidosis type II) - GEIMM
IGL015/00 (lymphoblast) - GEIMM
IGL015/01 (lymphoblast) - GEIMM
IGL015/96 (lymphoblast) - GEIMM
IGL015/97 (lymphoblast) - GEIMM
IGL015/98 (lymphoblast) - GEIMM
IGL015/99 (lymphoblast) - GEIMM
IGL016/00 (lymphoblast) - GEIMM
IGL016/01 (lymphoblast) - GEIMM
IGL016/96 (lymphoblast) - GEIMM
IGL016/97 (lymphoblast) - GEIMM
IGL016/98 (lymphoblast) - GEIMM
IGL016/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL017/00 (lymphoblast) - GEIMM
IGL017/01 (lymphoblast) - GEIMM
IGL017/96 (lymphoblast, glycogen storage disease II) - GEIMM
IGL017/97 (lymphoblast) - GEIMM
IGL017/98 (lymphoblast, mucopolysaccharidosis type IV A) - GEIMM
IGL017/99 (lymphoblast) - GEIMM
IGL018/96 (lymphoblast) - GEIMM
IGL018/97 (lymphoblast) - GEIMM
IGL018/98 (lymphoblast, Gaucher disease type II) - GEIMM
IGL018/99 (lymphoblast) - GEIMM
IGL019/00 (lymphoblast) - GEIMM
IGL019/96 (lymphoblast) - GEIMM
IGL019/97 (lymphoblast) - GEIMM
IGL019/98 (lymphoblast, Gaucher disease type II) - GEIMM
IGL019/99 (lymphoblast, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGL020/96 (lymphoblast) - GEIMM
IGL020/98 (lymphoblast, Wolman disease/cholesterol ester storage disease) - GEIMM
IGL020/99 (lymphoblast) - GEIMM
IGL021/96 (lymphoblast) - GEIMM
IGL021/98 (lymphoblast) - GEIMM
IGL021/99 (lymphoblast) - GEIMM
IGL022/00 (lymphoblast) - GEIMM
IGL022/96 (lymphoblast) - GEIMM
IGL022/98 (lymphoblast) - GEIMM
IGL022/99 (lymphoblast) - GEIMM
IGL023/00 (lymphoblast) - GEIMM
IGL023/96 (lymphoblast) - GEIMM
IGL023/98 (lymphoblast) - GEIMM
IGL023/99 (lymphoblast) - GEIMM
IGL024/00 (lymphoblast) - GEIMM
IGL024/96 (lymphoblast) - GEIMM
IGL024/98 (lymphoblast, Gaucher disease type I) - GEIMM
IGL024/99 (lymphoblast) - GEIMM
IGL025/00 (lymphoblast, SURF1) - GEIMM
IGL025/98 (lymphoblast, mucopolysaccharidosis type IV A) - GEIMM
IGL025/99 (lymphoblast) - GEIMM
IGL026/00 (lymphoblast) - GEIMM
IGL026/99 (lymphoblast) - GEIMM
IGL027/00 (lymphoblast) - GEIMM
IGL027/98 (lymphoblast, neuropathy, giant axonal) - GEIMM
IGL027/99 (lymphoblast) - GEIMM
IGL028/00 (lymphoblast) - GEIMM
IGL028/98 (lymphoblast, Gaucher disease type III) - GEIMM
IGL028/99 (lymphoblast) - GEIMM
IGL029/00 (lymphoblast, Gaucher disease type I) - GEIMM
IGL029/98 (lymphoblast) - GEIMM
IGL029/99 (lymphoblast) - GEIMM
IGL030/00 (lymphoblast, Gaucher disease type II) - GEIMM
IGL030/98 (lymphoblast) - GEIMM
IGL030/99 (lymphoblast) - GEIMM
IGL031/00 (lymphoblast) - GEIMM
IGL031/98 (lymphoblast) - GEIMM
IGL031/99 (lymphoblast, Gaucher disease type I) - GEIMM
IGL032/00 (lymphoblast) - GEIMM
IGL032/98 (lymphoblast) - GEIMM
IGL032/99 (lymphoblast) - GEIMM
IGL033/00 (lymphoblast) - GEIMM
IGL033/98 (lymphoblast) - GEIMM
IGL033/99 (lymphoblast) - GEIMM
IGL034/00 (lymphoblast, Niemann-Pick disease, type C) - GEIMM
IGL034/99 (lymphoblast) - GEIMM
IGL035/00 (lymphoblast, spastic paraparesis) - GEIMM
IGL035/99 (lymphoblast) - GEIMM
IGL036/99 (lymphoblast) - GEIMM
IGL037/99 (lymphoblast) - GEIMM
IGL038/99 (lymphoblast) - GEIMM
IGL039/99 (lymphoblast) - GEIMM
IGL040/99 (lymphoblast) - GEIMM
IGL041/99 (lymphoblast) - GEIMM
IGR-1 (melanoma) - DSMZ
IGR-37 (melanoma) - DSMZ
IGR-39 (melanoma) - DSMZ
IGROV-1 (ovary, carcinoma) - MIISB
IGV001/92 (chorionic villi, glycogen storage disease II) - GEIMM
IGV001/96 (chorionic villi, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGV001/99 (chorionic villi, mucolipidosis II) - GEIMM
IGV003/90 (chorionic villi, Tay-Sachs disease) - GEIMM
IGV003/93 (chorionic villi, fucosidosis) - GEIMM
IGV005/93 (chorionic villi, Niemann-Pick disease, type A) - GEIMM
IGV005/94 (chorionic villi, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGV006/99 (chorionic villi, Gaucher disease type II) - GEIMM
IGV008/94 (chorionic villi, mucolipidosis II) - GEIMM
IGV009/90 (chorionic villi, metachromatic leukodystrophy, late-infantile) - GEIMM
IGV009/96 (chorionic villi, Gaucher disease type II) - GEIMM
IGV009/99 (chorionic villi, Krabbe disease) - GEIMM
IGV011/92 (chorionic villi, Sjogren-Larsson syndrome) - GEIMM
IGV017/91 (chorionic villi, mucopolysaccharidosis type II) - GEIMM
IGV025/91 (chorionic villi, mucopolysaccharidosis type II) - GEIMM
IGV028/91 (chorionic villi, gangliosidosis, generalized GM1, type I) - GEIMM
IGV029/91 (chorionic villi, glycogen storage disease II) - GEIMM
IGV030/84 (chorionic villi, gangliosidosis, generalized GM1, type I) - GEIMM
IGV032/91 (chorionic villi, Sandhoff disease) - GEIMM
IM 9 (bone marrow, multiple myeloma) - ECACC
IM-9 (lymphoblastoid B cell, multiple myeloma) - DSMZ
IM-9 (bone marrow) - ICLC
IM-9 (bone marrow, multiple myeloma) - IZSBS
IM-9 (bone marrow, multiple myeloma) - SPBIC
IMG-1002 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-1003 (skin, fibroblast, progeria syndrome) - MWCMG
IMG-1006 (skin, fibroblast, osteogenesis imperfecta) - MWCMG
IMG-1007 (skin, fibroblast, Krabbe disease) - MWCMG
IMG-1008 (skin, fibroblast, Edwards' syndrome / trisomy 18) - MWCMG
IMG-1009 (skin, fibroblast, Edwards' syndrome / trisomy 18) - MWCMG
IMG-1018 (skin, fibroblast, Krabbe disease) - MWCMG
IMG-1019 (skin, fibroblast, Krabbe disease) - MWCMG
IMG-1021 XP4MO (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-1023 (skin, fibroblast, Krabbe disease) - MWCMG
IMG-1024 XP5MO (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-1025 (skin, fibroblast, Prader-Willi syndrome) - MWCMG
IMG-1027 (skin, fibroblast, basal cell nevus syndrome) - MWCMG
IMG-1028 XP6MO (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-1032 (skin, fibroblast, trisomy 21 / Down syndrome) - MWCMG
IMG-1035 (skin, fibroblast, trisomy 21 / Down syndrome) - MWCMG
IMG-1036 (skin, fibroblast, trisomy 21 / Down syndrome) - MWCMG
IMG-1037 (skin, fibroblast) - MWCMG
IMG-1038 (skin, fibroblast, trisomy 21 / Down syndrome) - MWCMG
IMG-1046 (skin, fibroblast, triploidy) - MWCMG
IMG-1048 (skin, fibroblast, poly-X syndrome) - MWCMG
IMG-1049 (skin, fibroblast, poly-X syndrome) - MWCMG
IMG-1053 (skin, fibroblast, osteogenesis imperfecta) - MWCMG
IMG-1054 (skin, fibroblast, osteogenesis imperfecta) - MWCMG
IMG-1062 (skin, fibroblast, triploidy) - MWCMG
IMG-1065 (skin, fibroblast, Marfan syndrome) - MWCMG
IMG-1066 (skin, fibroblast, Marfan syndrome) - MWCMG
IMG-1068 (skin, fibroblast, triplo-X syndrome) - MWCMG
IMG-1069 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-1070 (skin, fibroblast, triplo-X syndrome) - MWCMG
IMG-1080 XP7MO (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-1106 (skin, fibroblast, Cockayne syndrome) - MWCMG
IMG-1111 (skin, fibroblast, Marfan syndrome) - MWCMG
IMG-1112 (skin, fibroblast, metachromatic leukodystrophy) - MWCMG
IMG-1116 (skin, fibroblast, metachromatic leukodystrophy) - MWCMG
IMG-1117 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-1119 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-1121 (skin, fibroblast, metachromatic leukodystrophy) - MWCMG
IMG-1122 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-1123 (skin, fibroblast, metachromatic leukodystrophy) - MWCMG
IMG-1124 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-1126 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-1127 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-1129 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-1132 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-1134 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-1135 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-1136 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-1137 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-1140 (skin, fibroblast, Niemann-Pick disease) - MWCMG
IMG-1143 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-1144 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-1145 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-1146 (skin, fibroblast, Gaucher disease) - MWCMG
IMG-1149 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-1154 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-1156 (skin, fibroblast, mucolipidosis) - MWCMG
IMG-1161 (skin, fibroblast, mucopolysaccharidosis type IV B / Morquio syndrome) - MWCMG
IMG-1163 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-1164 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-1165 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-1176 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-1181 (skin, fibroblast, neuraminidase deficiency) - MWCMG
IMG-1211 (skin, fibroblast, triploidy) - MWCMG
IMG-1215 (skin, fibroblast, Beckwith-Wiedemann syndrome) - MWCMG
IMG-1216 (skin, fibroblast, retinoblastoma) - MWCMG
IMG-1217 XP8MO (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-1230 (skin, fibroblast, Down syndrome, mosaic) - MWCMG
IMG-1233 (skin, fibroblast, amyloidosis) - MWCMG
IMG-1234 (skin, fibroblast, amyloidosis) - MWCMG
IMG-1235 (skin, fibroblast, amyloidosis) - MWCMG
IMG-1239 (skin, fibroblast, Beckwith-Wiedemann syndrome) - MWCMG
IMG-1241 (skin, fibroblast, Down syndrome, mosaic) - MWCMG
IMG-1247 XP9MO (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-1250 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-1266 (skin, fibroblast, Down syndrome, mosaic) - MWCMG
IMG-1311 (skin, fibroblast, Patau syndrome / trisomy 13) - MWCMG
IMG-1344 (skin, fibroblast, Down syndrome, mosaic) - MWCMG
IMG-1347 (skin, fibroblast, Down syndrome, mosaic) - MWCMG
IMG-1359 (skin, fibroblast, YY-syndrome) - MWCMG
IMG-1360 (skin, fibroblast, YY-syndrome) - MWCMG
IMG-1366 (skin, fibroblast, Down syndrome, mosaic) - MWCMG
IMG-1370 (skin, fibroblast, Dubowitz syndrome) - MWCMG
IMG-1371 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-1373 (skin, fibroblast, Patau syndrome / trisomy 13) - MWCMG
IMG-1388 (skin, fibroblast, Down syndrome, mosaic) - MWCMG
IMG-1401 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1402 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1403 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1404 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1407 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1408 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1409 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1410 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1413 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1414 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1415 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1416 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1417 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1418 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1419 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1420 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1421 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-1425 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-1432 (skin, fibroblast, balanced chromosome translocation) - MWCMG
IMG-3003 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-375 (skin, fibroblast, trisomy 21 / Down syndrome) - MWCMG
IMG-478 (skin, fibroblast, triploidy) - MWCMG
IMG-484 XP2MO (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-492 (skin, fibroblast, YY-syndrome) - MWCMG
IMG-493 (skin, fibroblast, poly-X syndrome) - MWCMG
IMG-608 (skin, fibroblast, poly-X syndrome) - MWCMG
IMG-610 (skin, fibroblast, Gaucher disease) - MWCMG
IMG-630 (skin, fibroblast, Tay-Sachs disease) - MWCMG
IMG-636 (skin, fibroblast, scleroderma, familial progressive) - MWCMG
IMG-638 XP3LE (skin, fibroblast, pigmented xerodermoid) - MWCMG
IMG-639 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-649 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-650 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-653 (skin, fibroblast, thalassemia) - MWCMG
IMG-655 (skin, fibroblast, Niemann-Pick disease) - MWCMG
IMG-656 (skin, fibroblast, Tay-Sachs disease) - MWCMG
IMG-667 XP2LE (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-672 (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-673 (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-674 (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-675 (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-676 (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-678 (skin, fibroblast, Lesch-Nyhan syndrome) - MWCMG
IMG-679 (skin, fibroblast, Lesch-Nyhan syndrome) - MWCMG
IMG-683 (skin, fibroblast, Turner syndrome, mosaic) - MWCMG
IMG-688 (skin, fibroblast, Turner syndrome, mosaic) - MWCMG
IMG-691 (skin, fibroblast, Edwards' syndrome / trisomy 18) - MWCMG
IMG-694 (skin, fibroblast, cri du chat syndrome) - MWCMG
IMG-695 (skin, fibroblast, scleroderma, familial progressive) - MWCMG
IMG-706 (skin, fibroblast, progeria syndrome) - MWCMG
IMG-707 (skin, fibroblast, triploidy) - MWCMG
IMG-709 (skin, fibroblast, testicular feminization syndrome) - MWCMG
IMG-711 (skin, fibroblast, Tay-Sachs disease) - MWCMG
IMG-723 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-724 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-725 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-726 (skin, fibroblast, Sandhoff disease) - MWCMG
IMG-728 (skin, fibroblast, Sandhoff disease) - MWCMG
IMG-729 (skin, fibroblast, Sandhoff disease) - MWCMG
IMG-730 XP3MO (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-733 (skin, fibroblast, osteogenesis imperfecta) - MWCMG
IMG-734 (skin, fibroblast, trisomy 21 / Down syndrome) - MWCMG
IMG-736 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-740 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-743 (skin, fibroblast, spondyloepiphyseal dysplasia, congenital) - MWCMG
IMG-747 (skin, fibroblast, osteogenesis imperfecta) - MWCMG
IMG-758 (skin, fibroblast, Klinefelter syndrome) - MWCMG
IMG-759 (skin, fibroblast, Klinefelter syndrome) - MWCMG
IMG-761 (skin, fibroblast, thalassemia) - MWCMG
IMG-763 (skin, fibroblast, Klinefelter syndrome, mosaic) - MWCMG
IMG-765 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-766 (skin, fibroblast, Klinefelter syndrome) - MWCMG
IMG-767 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-768 (skin, fibroblast, Klinefelter syndrome, mosaic) - MWCMG
IMG-769 (skin, fibroblast, Turner syndrome, mosaic) - MWCMG
IMG-771 (skin, fibroblast, Klinefelter syndrome) - MWCMG
IMG-773 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-774 (skin, fibroblast, Klinefelter syndrome) - MWCMG
IMG-775 (skin, fibroblast, Klinefelter syndrome, mosaic) - MWCMG
IMG-776 (skin, fibroblast, Klinefelter syndrome) - MWCMG
IMG-778 (skin, fibroblast, Turner syndrome/noonan syndrome 1) - MWCMG
IMG-780 (skin, fibroblast, thalassemia) - MWCMG
IMG-785 (skin, fibroblast, thalassemia) - MWCMG
IMG-787 (skin, fibroblast, thalassemia) - MWCMG
IMG-788 (skin, fibroblast, thalassemia) - MWCMG
IMG-796 (skin, fibroblast, Edwards' syndrome / trisomy 18) - MWCMG
IMG-797 (skin, fibroblast, Edwards' syndrome / trisomy 18) - MWCMG
IMG-807 (skin, fibroblast, thalassemia) - MWCMG
IMG-809 (skin, fibroblast, thalassemia) - MWCMG
IMG-810 (skin, fibroblast, thalassemia) - MWCMG
IMG-811 (skin, fibroblast, thalassemia) - MWCMG
IMG-817 (skin, fibroblast, X chromosome anomaly) - MWCMG
IMG-819 (skin, fibroblast, mucopolysaccharidosis type III B) - MWCMG
IMG-819 XP8CA (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-823 (skin, fibroblast, Tay-Sachs disease) - MWCMG
IMG-824 (skin, fibroblast, Lesch-Nyhan syndrome) - MWCMG
IMG-826 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-827 (skin, fibroblast, mannosidosis, alpha b, lysosomal) - MWCMG
IMG-831 (skin, fibroblast, X chromosome anomaly) - MWCMG
IMG-847 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-856 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-857 (skin, fibroblast, trisomy 22) - MWCMG
IMG-858 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-884 (skin, fibroblast, metachromatic leukodystrophy) - MWCMG
IMG-895 (skin, fibroblast, Tay-Sachs disease) - MWCMG
IMG-905 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-906 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-907 (skin, fibroblast, Tay-Sachs disease) - MWCMG
IMG-908 (skin, fibroblast, mucopolysaccharidosis type IV B / Morquio syndrome) - MWCMG
IMG-909 (skin, fibroblast, mucopolysaccharidosis type IV B / Morquio syndrome) - MWCMG
IMG-911 (skin, fibroblast, mucopolysaccharidosis type IV B / Morquio syndrome) - MWCMG
IMG-915 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-920 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-921 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-925 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - MWCMG
IMG-926 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-933 (skin, fibroblast, mucopolysaccharidosis type IV B / Morquio syndrome) - MWCMG
IMG-934 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-935 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-936 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-938 (skin, fibroblast, progeria syndrome) - MWCMG
IMG-939 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-940 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-941 (skin, fibroblast, mucopolysaccharidosis type III A) - MWCMG
IMG-944 (skin, fibroblast, trisomy 21 / Down syndrome) - MWCMG
IMG-946 (skin, fibroblast, trisomy 21 / Down syndrome) - MWCMG
IMG-947 (skin, fibroblast, trisomy 21 / Down syndrome) - MWCMG
IMG-948 (skin, fibroblast, trisomy 21 / Down syndrome) - MWCMG
IMG-949 (skin, fibroblast, Patau syndrome / trisomy 13) - MWCMG
IMG-962 (skin, fibroblast, Ehlers-Danlos syndrome) - MWCMG
IMG-963 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-964 (skin, fibroblast, Gaucher disease) - MWCMG
IMG-965 (skin, fibroblast, metachromatic leukodystrophy) - MWCMG
IMG-966 (skin, fibroblast, metachromatic leukodystrophy) - MWCMG
IMG-968 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-969 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-971 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-972 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-973 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-978 (skin, fibroblast, poly-X syndrome) - MWCMG
IMG-982 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-983 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-984 (skin, fibroblast, mucopolysaccharidosis type II) - MWCMG
IMG-985 (skin, fibroblast, metachromatic leukodystrophy) - MWCMG
IMG-988 (skin, fibroblast, Krabbe disease) - MWCMG
IMG-989 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-990 XP3Br2 (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-991 XP3ORO (skin, fibroblast, xeroderma pigmentosum) - MWCMG
IMG-994 (skin, fibroblast, metachromatic leukodystrophy) - MWCMG
IMG-995 (skin, fibroblast, mucopolysaccharidosis type III B) - MWCMG
IMG-996 (skin, fibroblast, mucopolysaccharidosis type I / Hurler disease) - MWCMG
IMG-997 (skin, fibroblast, Kartagener syndrome X) - MWCMG
IMG-998 (skin, fibroblast, Niemann-Pick disease) - MWCMG
IMG-999 (skin, fibroblast, gangliosidosis, generalized GM1, type I) - MWCMG
IMR 32 (abdomen, neuroblastoma) - ECACC
IMR 32 (neuroblastoma) - IZSBS
IMR-32 (neuroblastoma) - BOHIC
IMR-32 (neuroblastoma) - DSMZ
IMR-32 (neuroblastoma) - GEICV
IMR-32 (neuroblastoma) - ICLC
IMR-32 (neuroblastoma) - MIISA
IMR-32 (neuroblastoma) - MIUEP
IMR-32 (neuroblastoma) - RMUPG
IMR-32 (neuroblastoma) - SPBIC
IMR-5 (neuroblastoma) - ICLC
IMR-90 (lung, embryonic) - ECACC
IMR-90 (lung, embryonic) - IZSBS
INT 407 (intestine, embryonic) - ECACC
Intestine 407 (intestine, embryonic) - IZSBS
Intestine 407 (intestine, embryonic) - MIUCC
Intestine 407 (intestine, embryonic) - PRUMB
IP1PV (skin, fibroblast, incontinentia pigmenti) - PVCGU
IP2PV (skin, fibroblast) - PVCGU
IPC-298 (melanoma) - DSMZ
IS94 (lymphocyte) - GGB
IST-EBV-TW1.1 (lymphocyte, B) - ICLC
IST-EBV-TW1.2 (lymphocyte, B) - ICLC
IST-EBV-TW2.1 (lymphocyte, B) - ICLC
IST-EBV-TW2.2 (lymphocyte, B) - ICLC
IST-EBV-TW3.1 (lymphocyte, B) - ICLC
IST-EBV-TW3.2 (lymphocyte, B) - ICLC
IST-EBV-TW4A (lymphocyte, B) - ICLC
IST-EBV-TW4B (lymphocyte, B) - ICLC
IST-EBV-TW5A (lymphocyte, B) - ICLC
IST-EBV-TW5B (lymphocyte, B) - ICLC
IST-EBV-TW6A (lymphocyte, B) - ICLC
IST-EBV-TW6B (lymphocyte, B) - ICLC
IST-MEL1 (skin, melanoma) - ICLC
IST-MEL2 (skin, melanoma) - ICLC
IST-MEL3 (skin, melanoma) - ICLC
IST-MELA 16 (subcutaneous metastasis, melanoma, metastatic) - ICLC
IST-MES1 (pleural effusion, mesothelioma) - ICLC
IST-MES2 (pleural effusion, mesothelioma) - ICLC
IST-SL1 (lung, carcinoma, small cell) - ICLC
IST-SL2 (lung, carcinoma, small cell) - ICLC
IV95 (lymphocyte, trisomy 21 / Down syndrome) - GGB

For information, get in touch with:
IRCCS Ospedale Policlinico San Martino
Largo Rosanna Benzi, 10 - I-16132 Genova - Italy
Dott.ssa Paola Visconti
Email: paola.visconti@hsanmartino.it

If you want to cite CLDB and HyperCLDB, please use the following reference:

P. Romano, A. Manniello, O. Aresu, M. Armento, M. Cesaro, B. Parodi.
Cell Line Data Base: structure and recent improvements towards molecular authentication of human cell lines.
Nucleic Acids Research 2009 37(Database issue):D925-D932.
DOI: doi:10.1093/nar/gkn730; PMID: 18927105