Female carriers of Duchenne muscular dystrophy: a dilemma
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1987.tb02810.x/fullpdf
Reference16 articles.
1. A study of possible heterogenecity in Duchenne muscular dystrophy;Emery;Clin. Genet.,1979
2. X-chromo-some inactivation studied by injection of a single cell into the mouse blastocyst;Gardner;Nature,1971
3. Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twins;Gomez;Neurology,1977
4. Isolation of probes detecting RFLPs from X-chromosome specific libraries. Potential use for diagnosis of DMD;Hotter;Hum. Genet.,1985
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. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers;American Journal of Medical Genetics;1998-12-04
2. Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation;American Journal of Medical Genetics;1994-08-15
3. Discordance of muscular dystrophy in monozygotic female twins: Evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy;American Journal of Medical Genetics;1991-09-01
4. Recent Advances in Duchenne and Becker Muscular Dystrophy;Neurologic Clinics;1988-08
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