Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometry
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference20 articles.
1. Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene.
2. PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs
3. Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations.
4. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
5. Dystrophin is transcribed in brain from a distant upstream promoter.
Cited by 6 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. Strategy for Comprehensive Molecular Testing for Duchenne and Becker Muscular Dystrophies;Genetic Testing;2006-01
2. Denaturing HPLC Coupled with Multiplex PCR for Rapid Detection of Large Deletions in Duchenne Muscular Dystrophy Carriers;Clinical Chemistry;2005-07-01
3. Rapid identification of female carriers of DMD/BMD by quantitative real-time PCR;Human Mutation;2004
4. X-linked recessive Menkes disease: carrier detection in the case of a partial gene deletion;Clinical Genetics;2002-12
5. Comparative analysis of PCR-deletion detection and immunohistochemistry in Brazilian Duchenne and Becker muscular dystrophy patients;American Journal of Medical Genetics;2001
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