Prenatal Diagnosis of Duchenne Muscular Dystrophy in the Japanese Population by Fluorescent CA Repeat Polymorphisms Analysis
Author:
Publisher
Wiley
Subject
Obstetrics and Gynaecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1447-0756.1997.tb00873.x/fullpdf
Reference16 articles.
1. Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention;Moser;Hum Genet,1981
2. Deletion screening of the Duchenne muscular dystrophy via multiplex DNA amplification;Chamberlain;Nucleic Acids Res,1988
3. Detection of 98% of DMD/BMD gene detections by polymerase chain reaction;Beggs;Hum Genet,1990
4. Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy;Robert;Nucleic Acids Res,1989
5. Prenatal diagnosis of Duchenne muscular dystrophy analysis by the polymerase chain reaction analysis;Katayama;Fetal Diagn Ther,1994
Cited by 3 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. Prenatal diagnosis of duchenne/becker muscular dystrophy by short tandem repeat segregation analysis in argentine families;Muscle & Nerve;2011-02-08
2. A Larger Spectrum of Intragenic Short Tandem Repeats Improves Linkage Analysis and Localization of Intragenic Recombination Detection in the Dystrophin Gene;The Journal of Molecular Diagnostics;2007-02
3. Analysis of dinucleotide repeat loci of dystrophin gene for carrier detection, germline mosaicism and de novo mutations in Duchenne muscular dystrophy;Clinical Genetics;2000-09
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