Brother/sister siblings affected with Hunter disease: evidence for skewed X chromosome inactivation-Reference-Cited by-同舟云学术

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Brother/sister siblings affected with Hunter disease: evidence for skewed X chromosome inactivation

Published:2008-06-28 Issue:2 Volume:53 Page:96-101
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Sukegawa Kazuko,Matsuzaki Tetuo,Fukuda Seiji,Masuno Mitsuo,Fukao Toshiyuki,Kokuryu Mie,Iwata Shoko,Tomatsu Shunji,Orii Tadao,Kondo Naomi

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1998.tb02654.x/fullpdf

Reference27 articles.

1. Gene action in the X-chromosome of the mouse;Lyon;Nature,1961

2. The normal human female as a mosaic of X-chromosome activity: studies using the gene for G-6-PD-deficiency as a marker;Beutler;Proc Natl Acad Sci USA,1962

3. Molecular analysis of a female Lesch-Nyhan patient;Ogasawara;J Clin Invest,1989

4. Novel nonsense mutation in the hypoxanthine guanine phosphoribosyltransferase gene and nonrandom X-inactivation causing Lesch-Nyhan syndrome in a female patient;Aral;Hum Mutat,1996

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