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- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- A matter of excessive hair growth
- Congenital atrichia and hypotrichosis
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Bimatoprost solution 0·03% topical application to the eyelid margin for the treatment of eyelash hypotrichosis
- Notes from the Editor Emeritus: Medical therapy for hair loss: what we know and what we need to find out
- Marie-unna hereditary hypotrichosis
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
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