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- Monilethrix: A rare hereditary condition
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- ST Premature Graying Hair in Seven Years Old Children
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
- Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis
- Polycystic Ovaries Are Inherited as an Autosomal Dominant Trait: Analysis of 29 Polycystic Ovary Syndrome and 10 Control Families
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- Heterozygous <i>KRT32</i> variant is responsible for autosomal dominant loose anagen hair syndrome
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