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- Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Familial congenital generalized hypertrichosis
- Congenital hypotrichosis due to short anagen
- A new type of pachyonychia congenita.
- Alopezien und Hypotrichosen im Kindesalter
- Woolly hair generalizado: caso clínico e revisão da literatura
- Clinical and molecular genetic studies in hereditary hair loss
- Office Diagnosis of Hair Shaft Defects
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie-unna hereditary hypotrichosis
- Two females with hair loss
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Acquired Uncombable Hair
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Congenital atrichia and hypotrichosis
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis