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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
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