DOIAbstract
Identity Defect in melanocyte development; one of the first genetic disorders for which a pedigree was presented in 1786. Inheritance Autosomal dominant; frequency is about 2.5/105 newborns
Identity Defect in melanocyte development; one of the first genetic disorders for which a pedigree was presented in 1786. Inheritance Autosomal dominant; frequency is about 2.5/105 newborns
In this article we describe the rapid advances made in the molecular genetics of three inherited pig...
Copyright © 2013 Yong-jia Yang et al. This is an open access article distributed under the Creative ...
A 4-year-old mentally retarded girl had congenital depigmentations of ventrolateral parts of the che...
Piebaldism is an autosomal dominant genetic disorder of pigmentation characterized by congenital pat...
T Piebaldism is a rare, autosomal dominant disorder characterized by the congenital absence of melan...
Piebaldism is an autosomal dominant genetic disorder of pigmentation characterized by congenital pat...
Piebaldism is an uncommon, autosomal dominant, congenital, stable leukoderma associated with white f...
Piebaldism is an autosomal dominant genetic pigmentary disorder, characterized by congenital white h...
Piebaldism is an autosomal dominant disorder, characterized by congenital leukoderma typically on th...
Piebaldism is an autosomal dominant congenital disorder in pigment as a result of mutations in KIT g...
Human piebald trait is an autosomal dominant defect in mela-nocyte development characterized by patc...
Piebaldism is an uncommon genetic defect where anomalies in skin-pigmentation are limited to hair an...
Human piebaldism is a rare autosomal dominant disorder that comprises congenital patchy depigmentati...
Subcellular defects of hypomelanosis in tuberous sclerosis (TS) (28 subjects) were compared by light...
A 4-year-old mentally retarded girl had congenital depigmentations of ventrolateral parts of the che...
In this article we describe the rapid advances made in the molecular genetics of three inherited pig...
Copyright © 2013 Yong-jia Yang et al. This is an open access article distributed under the Creative ...
A 4-year-old mentally retarded girl had congenital depigmentations of ventrolateral parts of the che...
Piebaldism is an autosomal dominant genetic disorder of pigmentation characterized by congenital pat...
T Piebaldism is a rare, autosomal dominant disorder characterized by the congenital absence of melan...
Piebaldism is an autosomal dominant genetic disorder of pigmentation characterized by congenital pat...
Piebaldism is an uncommon, autosomal dominant, congenital, stable leukoderma associated with white f...
Piebaldism is an autosomal dominant genetic pigmentary disorder, characterized by congenital white h...
Piebaldism is an autosomal dominant disorder, characterized by congenital leukoderma typically on th...
Piebaldism is an autosomal dominant congenital disorder in pigment as a result of mutations in KIT g...
Human piebald trait is an autosomal dominant defect in mela-nocyte development characterized by patc...
Piebaldism is an uncommon genetic defect where anomalies in skin-pigmentation are limited to hair an...
Human piebaldism is a rare autosomal dominant disorder that comprises congenital patchy depigmentati...
Subcellular defects of hypomelanosis in tuberous sclerosis (TS) (28 subjects) were compared by light...
A 4-year-old mentally retarded girl had congenital depigmentations of ventrolateral parts of the che...
In this article we describe the rapid advances made in the molecular genetics of three inherited pig...
Copyright © 2013 Yong-jia Yang et al. This is an open access article distributed under the Creative ...
A 4-year-old mentally retarded girl had congenital depigmentations of ventrolateral parts of the che...
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