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Research 991–1000 of 1000+
- Marie-unna hereditary hypotrichosis
- Familial congenital generalized hypertrichosis
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- Genes for intermediate filament proteins and the draft sequence of the human genome
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Overexpression of Hoxc13 in differentiating keratinocytes results in downregulation of a novel hair keratin gene cluster and alopecia
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family