XY translocation in a boy with ichthyosis, hypogonadism, short stature and mental retardation
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1991.tb03004.x/fullpdf
Reference8 articles.
1. Y-to-X chromosome translocation observed in two generations;Akesson;Hum. Genet.,1980
2. X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulfatase gene and translocation of its Y pseudogene;Ballabio;Clin. Genet.,1988
3. Y to X translocation in man;Berghe;Hum. Genet.,1977
4. A case of X;Y translocation which maps the Xg locus to Xp24→pter;Boyd;J. Med. Genet.,1981
5. A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardation;Metaxotou;Clin. Genet.,1983
Cited by 4 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. Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis;Clinical Genetics;2000-06
2. Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14);American Journal of Medical Genetics;1999-11-19
3. Phenotype/Karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases;American Journal of Medical Genetics;1994-11-01
4. Absent chondrodysplasia punctata in a male with an Xp terminal deletion involving the putative region for CDPX1 locus;American Journal of Medical Genetics;1993-01-01
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