Deletions, duplications and novel restriction fragment length polymorphism in Duchenne and Becker muscular dystrophies
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03676.x/fullpdf
Reference25 articles.
1. Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy;Boyd;Clin Genet,1986
2. Point mutation in the human dystrophin gene: identification through Western blot analysis;Bulman;Genomics,1991
3. A cDNA clone from the Duchenne/Becker muscular dystrophy gene;Bughes;Nature,1987
4. A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene;Burmcister;Genomics,1988
5. Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients;Cross;EMBO J,1987
Cited by 5 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. Multiplex Ligation-dependent Probe Amplification Identification of Deletions and Duplications of the Duchenne Muscular Dystrophy Gene in Taiwanese Subjects;Journal of the Formosan Medical Association;2007-05
2. A different spectrum of DMD gene mutations in local Chinese patients with Duchenne/Becker muscular dystrophy;Chinese Medical Journal;2006-07
3. More deletions in the 5′ region than in the central region of the dystrophin gene were identified among filipino duchenne and becker muscular dystrophy patients;American Journal of Medical Genetics;1995-11-06
4. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients;American Journal of Medical Genetics;1994-02-15
5. A molecular survey of Israeli Duchenne and Becker muscular dystrophy patients;Biomedicine & Pharmacotherapy;1994-01
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