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- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Insertional mutation of the hairless locus on mouse Chromosome 14
- The Near-Naked Hairless (Hr) Mutation Disrupts Hair Formation but Is Not Due to a Mutation in the Hairless Coding Region
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- A missense mutation in Lama3 causes androgen alopecia
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- The role of vitamin D receptor mutations in the development of alopecia