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- 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.
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Congenital atrichia with papular lesions
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Congenital atrichia with papular lesions
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- Papular atrichia
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- Hairless: A nuclear receptor corepressor essential for skin function
- Reply
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Congenital atrichia associated with nevus flammeus: A rare association
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Atrichia with papular lesions
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Disease causing homozygous variants in the human hairless gene
- Biology and Genetics of Hair
- Alopecia totalis in an infant
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Congenital Atrichia: A Case Report
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis