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Search Results for - AMISH BRITTLE HAIR BRAIN SYNDROME

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ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1; TTDN1 | TTDN1 GENE; TTDN1 (C7ORF11)
 
DNA
 
Fibroblast
 
 
 
 
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1; TTDN1 | TTDN1 GENE; TTDN1 (C7ORF11)
 
Fibroblast
 
 
 
 
 
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1; TTDN1 | TTDN1 GENE; TTDN1 (C7ORF11)
 
Fibroblast
 
 
 
 
 
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1; TTDN1 | TTDN1 GENE; TTDN1 (C7ORF11)
 
Fibroblast
 
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
 
LCL
 
B-Lymphocyte
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
 
LCL
 
B-Lymphocyte
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
 
Fibroblast
 
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
 
LCL
 
B-Lymphocyte
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
 
Fibroblast
 
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
 
Fibroblast
 
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED | EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 2; ERCC2
 
DNA
 
Fibroblast
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED | EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 2; ERCC2
 
Fibroblast
 
 
 
 
 
ELLIS-VAN CREVELD SYNDROME; EVC
 
LCL
 
B-Lymphocyte
 
 
 
 
CLEFT LIP/PALATE - ECTODERMAL DYSPLASIA SYNDROME; CLPED1 | POLIOVIRUS RECEPTOR-LIKE 1; PVRL1
 
LCL
 
B-Lymphocyte
 
 
 
 
CLEFT LIP/PALATE - ECTODERMAL DYSPLASIA SYNDROME; CLPED1 | POLIOVIRUS RECEPTOR-LIKE 1; PVRL1
 
Fibroblast
 
 
 
 
 
TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3
 
LCL
 
B-Lymphocyte
 
 
 
 
TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3
 
LCL
 
B-Lymphocyte
 
 
 
 
CARTILAGE-HAIR HYPOPLASIA; CHH
 
Fibroblast
 
 
 
 
 
CARTILAGE-HAIR HYPOPLASIA; CHH
 
Fibroblast
 
 
 
 
 
COCKAYNE SYNDROME TYPE UNSPECIFIED
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
CARTILAGE-HAIR HYPOPLASIA; CHH
 
LCL
 
B-Lymphocyte
 
 
 
 
CARTILAGE-HAIR HYPOPLASIA; CHH
 
LCL
 
B-Lymphocyte
 
 
 
 
CARTILAGE-HAIR HYPOPLASIA; CHH
 
LCL
 
B-Lymphocyte
 
 
 
 
CARTILAGE-HAIR HYPOPLASIA; CHH
 
LCL
 
B-Lymphocyte
 
 
 
 
CARTILAGE-HAIR HYPOPLASIA; CHH
 
LCL
 
B-Lymphocyte
 
 
 
 
CARTILAGE-HAIR HYPOPLASIA; CHH
 
LCL
 
B-Lymphocyte
 
 
 
 
TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 | GENERAL TRANSCRIPTION FACTOR IIH, POLYPEPTIDE 5; GTF2H5
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
XXY SYNDROME; KLINEFELTER SYNDROME
 
DNA
 
LCL
 
 
 
 
XXY SYNDROME; KLINEFELTER SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD | TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED | EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 2; ERCC2
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | APPARENTLY HEALTHY INDIVIDUAL
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
DNA
 
LCL
 
 
 
 
MENKES SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
MENKES SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
 
Fibroblast
 
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
 
LCL
 
B-Lymphocyte
 
 
 
 
COCKAYNE SYNDROME TYPE UNSPECIFIED
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
WERNER SYNDROME; WRN REPLICATION FOCUS-FORMING ACTIVITY 1, INCLUDED; FFA1, INCLUDED
 
LCL
 
B-Lymphocyte

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