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- 1 October 2000
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 115 (4) , 762-763
- https://doi.org/10.1046/j.1523-1747.2000.00124-2.x
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
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- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesionsExperimental Dermatology, 2000
- Clustering of mutations associated with mild Marfan-like phenotypes in the 3? region ofFBN1 suggests a potential genotype-phenotype correlationAmerican Journal of Medical Genetics, 2000
- Atrichia with Papular Lesions Resulting from a Nonsense Mutation Within the Human Hairless GeneJournal of Investigative Dermatology, 1999
- Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlationBritish Journal of Dermatology, 1999
- Identification of a Genetic Defect in the Hairless Gene in Atrichia with Papular Lesions: Evidence for Phenotypic Heterogeneity among Inherited AtrichiasAmerican Journal of Human Genetics, 1999
- Atrichia with papular lesions maps to 8p in the region containing the human hairless geneAmerican Journal of Medical Genetics, 1998
- Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humansExperimental Dermatology, 1998
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish TravellersAmerican Journal of Human Genetics, 1998
- Alopecia Universalis Associated with a Mutation in the Human hairless GeneScience, 1998