Genomic Organization of the Human Hairless Gene (HR) and Identification of a Mutation Underlying Congenital Atrichia in an Arab Palestinian Family
Open Access
- 1 March 1999
- Vol. 56 (2) , 141-148
- https://doi.org/10.1006/geno.1998.5699
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Molecular Basis for the rhino (hrrh-8J)Phenotype: A Nonsense Mutation in the MousehairlessGeneGenomics, 1998
- Molecular basis of a novel rhino (hrrhChr) phenotype: a nonsense mutation in the mouse hairless geneExperimental Dermatology, 1998
- Molecular basis for the rhino Yurlovo (hrrhY) phenotype: severe skin abnormalities and female reproductive defects associated with an insertion in the hairless geneExperimental 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
- A Gene for Universal Congenital Alopecia Maps to Chromosome 8p21-22American Journal of Human Genetics, 1998
- Location of stem cells of human hair follicles by clonal analysisCell, 1994
- The secret life of the hair follicleTrends in Genetics, 1992
- Analysis of a murine male germ cell‐specific transcript that encodes a putative zinc finger proteinMolecular Reproduction and Development, 1991
- Autosomal recessive inheritance of atrichia congenitaClinical Genetics, 1980
- The Skin of Hairless Mice. I. The Formation of Cysts and the Distribution of LipidsJournal of Investigative Dermatology, 1952