Molecular-genetic study of Duchenne and Becker muscular dystrophies: Deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females-Reference-Cited by-同舟云学术

Molecular-genetic study of Duchenne and Becker muscular dystrophies: Deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females

Published:1989-12 Issue:4 Volume:34 Page:555-561
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Sugino Shigeto,Fujishita Satoshi,Kamimura Naohisa,Matsumoto Tadashi,Wapenaar Martin C.,Deng Han-Xiang,Shibuya Noritoshi,Miike Teruhisa,Niikawa Norio

Publisher

Wiley

Subject

Genetics(clinical)

Reference25 articles.

1. Diagnosis of Duchenne and Becker muscular dystrophies by DNA polymorphism

2. Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies

3. A cDNA clone from the Duchenne/Becker muscular dystrophy gene

Cited by 24 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. Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection;Clinical Genetics;2008-06-28

2. A different spectrum of DMD gene mutations in local Chinese patients with Duchenne/Becker muscular dystrophy;Chinese Medical Journal;2006-07

3. High frequency of de novo deletions in Mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling;Clinical Genetics;1999-05

4. Pattern of deletions of the dystrophin gene in Mexican Duchenne/Becker muscular dystrophy patients: The use of new designed primers for the analysis of the major deletion “hot spot” region;American Journal of Medical Genetics;1997-06-13

5. Are there ethnic differences in deletions in the dystrophin gene?;AM J MED GENET;1997