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Research 6
- Current Genetics in Hair Diseases
- Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology
- Congenital hair loss disorders: Rare, but not too rare
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis