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Search Results for - STEELY HAIR DISEASE

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ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
DNA
 
LCL
 
 
 
 
MENKES SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
MENKES SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
MENKES SYNDROME | APPARENTLY HEALTHY INDIVIDUAL
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
LCL
 
B-Lymphocyte
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
DNA
 
LCL
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
DNA
 
Fibroblast
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
Fibroblast
 
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
DNA
 
Fibroblast
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
DNA
 
Fibroblast
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
DNA
 
Fibroblast
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
DNA
 
Fibroblast
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
DNA
 
Fibroblast
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
DNA
 
Fibroblast
 
 
 
 
MENKES SYNDROME | ATPASE, CU(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
 
DNA
 
Fibroblast
 
 
 
 
CHROMOSOME X REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS
 
Somatic cell hybrid
 
 
 
 
 
CHROMOSOME X REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS
 
DNA
 
Somatic cell hybrid
 
 
 
 
PERSONAL GENOME PROJECT
 
LCL
 
B-Lymphocyte
 
 
 
 
PERSONAL GENOME PROJECT
 
LCL
 
B-Lymphocyte
 
 
 
 
SIALIC ACID STORAGE DISEASE; SIASD
 
Fibroblast
 
 
 
 
 
CARTILAGE-HAIR HYPOPLASIA; CHH
 
Fibroblast
 
 
 
 
 
CARTILAGE-HAIR HYPOPLASIA; CHH
 
Fibroblast
 
 
 
 
 
PERSONAL GENOME PROJECT
 
LCL
 
B-Lymphocyte
 
 
 
 
VITILIGO | HASHIMOTO THYROIDITIS
 
LCL
 
B-Lymphocyte
 
 
 
 
VITILIGO | HASHIMOTO THYROIDITIS
 
LCL
 
B-Lymphocyte
 
 
 
 
PELIZAEUS-MERZBACHER-LIKE DISEASE, TYPE UNKNOWN
 
DNA
 
LCL
 
 
 
 
PERSONAL GENOME PROJECT
 
LCL
 
B-Lymphocyte
 
 
 
 
HERMANSKY-PUDLAK SYNDROME; HPS | HPS1 GENE; HPS1
 
DNA
 
LCL
 
 
 
 
PELIZAEUS-MERZBACHER-LIKE DISEASE, TYPE UNKNOWN
 
LCL
 
B-Lymphocyte
 
 
 
 
TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED
 
Fibroblast
 
Skin, Unspecified

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