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- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Woolly hair nevus
- A rare case of woolly hair with unusual associations
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- [Wooly hair syndrome. Clinical and microscopic study].
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- WOOLY HAIR PALMOPLANTAR KERATODERMA : A CASE REPORT
- Clinicopathological insights into the phenotypic variation of autosomal recessive hypotrichosis/wooly hair by c.736T>A LIPH mutation
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
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