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- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- 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 resulting from a novel insertion mutation in the human hairless gene
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Papular atrichia
- Atrichia with papular lesions
- Disease causing homozygous variants in the human hairless gene
- Molecular basis of congenital atrichia in humans and mice.
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Congenital atrichia with papular lesions
- Biology and Genetics of Hair
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Hairless: A nuclear receptor corepressor essential for skin function
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- 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
- Congenital atrichia with papular lesions
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Morphological Approach to Hair Disorders
- A Newborn With Hair Loss