Identification of duchenne muscular dystrophy genomic probe P20 constant Taq1 fragment corresponding to the EcoRV and Msp1 polymorphisms-Reference-Cited by-同舟云学术

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Identification of duchenne muscular dystrophy genomic probe P20 constant Taq1 fragment corresponding to the EcoRV and Msp1 polymorphisms

Published:1991-01 Issue:1 Volume:11 Page:63-67
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Laing N. G.,Walker A. P.,Akkari P. A.,Chandler D. C.,Layton M. G.,Mears M. E.,Yamada T.,Bartlett R. J.,Pericak-Vance M. A.,Hung W.-Y.,Wapenaar M. C.,van Ommen G.,Roses A. D.,Kakulas B. A.

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference18 articles.

1. Prenatal detection of an inherited Duchenne muscular dystrophy deletion allele

2. Duchenne muscular dystrophy: High frequency of deletions

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

4. Prenatal diagnosis in a female carrying a deletion close to the duchenne locus

Cited by 2 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. Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia;Prenatal Diagnosis;1993-05

2. A TaqI map of the dystrophin gene useful for deletion and carrier status analysis.;Journal of Medical Genetics;1992-01-01

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