Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: evidence for an ancestral pseudoautosomal gene?
Author:
Affiliation:
1. Genetics Laboratory, South Parks Road, Oxford OX1 3QU, UK
2. International Institute for Genetics and Biophysics, Via G. Marcom, Naples, Italy
Abstract
Publisher
The Company of Biologists
Subject
Developmental Biology,Molecular Biology
Link
http://journals.biologists.com/dev/article-pdf/101/Supplement/127/1120112/127.pdf
Cited by 25 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogene;Clinical Genetics;2008-06-28
2. The Genetic Basis for Sex Differences in Human Behaviour: Role of the Sex Chromosomes;Annals of Human Genetics;2004-05
3. Xp contiguous gene syndromes: from clinical observation to disease gene identification;Chromosomes Today;2000
4. X-linked ichthyosis: an update;British Journal of Dermatology;1999-10
5. Characterization ofCxorf5(71-7A), a Novel Human cDNA Mapping to Xp22 and Encoding a Protein Containing Coiled-Coil α-Helical Domains;Genomics;1998-07
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