Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy-Reference-Cited by-同舟云学术

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Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy

Published:1988-07 Issue:6 Volume:8 Page:427-437
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Speer Marcy C.,Pericak-Vance Margaret A.,Yamaoka Larry H.,Koh James,Hung Wu-Yen,Gaskell Peter C.,Vance Jeffery M.,Bartlett Richard J.,Roses Allen D.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference20 articles.

1. Hemophilia A

2. PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs

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

4. Duchenne muscular dystrophy: High frequency of deletions

5. Huntington disease: Estimation of heterozygote status using linked genetic markers

Cited by 4 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. Dystrophinopathies;Seminars in Pediatric Neurology;1996-06

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

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

4. Identification of duchenne muscular dystrophy genomic probe P20 constant Taq1 fragment corresponding to the EcoRV and Msp1 polymorphisms;Prenatal Diagnosis;1991-01

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