Report on the 16th ENMC workshop—Carrier diagnosis of Duchenne and Becker muscular dystrophy-Reference-Cited by-同舟云学术

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Report on the 16th ENMC workshop—Carrier diagnosis of Duchenne and Becker muscular dystrophy

Published:1993-01 Issue:3 Volume:3 Page:241-242
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Abbs Stephen,Bobrow Martin

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference1 articles.

1. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms;Clemens;Am J Hum Genet,1991

Cited by 8 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. Use of the MLPA Assay in the Molecular Diagnosis of Gene Copy Number Alterations in Human Genetic Diseases;International Journal of Molecular Sciences;2012-03-08

2. Detection of deletions and duplications in the Duchenne muscular dystrophy gene by the molecular method MLPA in the first Argentine affected families;Genetics and Molecular Research;2008

3. Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA);Human Genetics;2005-04-20

4. Genetic Testing;New England Journal of Medicine;2002-12-05

5. The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol.;Journal of Medical Genetics;1997-10-01

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