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Research 21
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Two females with hair loss
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Biology and Genetics of Hair
- Molecular Genetics of Alopecias
- Disease causing homozygous variants in the human hairless gene
- Hair loss and its management in children
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Alopezien und Hypotrichosen im Kindesalter
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Genetic Hair Disorders: A Review
- Current Genetics in Hair Diseases
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- Marie-unna hereditary hypotrichosis
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity