Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysis-Reference-Cited by-同舟云学术

Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysis

Published:2008-06-28 Issue:4 Volume:27 Page:383-391
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Kingston H. M.,Sarfarazi M.,Newcombe R. G.,Willis N.,Harper P. S.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1985.tb02280.x/fullpdf

Reference11 articles.

1. Plasma pyruvate kinase and creatine kinase activity in Becker muscular dystrophy;Aston;J. Neurol. Sci.,1984

2. Utility and efficiency of linked marker genes for genetic counselling: Identification of linkage phase by offspring phenotypes;Chakravarti;Am. J. Hum. Genet.,1982

3. Detection of carriers of benign X-linked muscular dystrophy;Emery;Br. Med. J.,1967

4. The use of linked DNA polymorphism for genotype prediction in families with Duchenne muscular dystrophy;Harper;J. Med. Genet.,1983

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1. Cardiac involvement in Becker muscular dystrophy;Canadian Journal of Cardiology;2008-10

2. Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results;Clinical Genetics;2008-06-28

3. A survey of manifesting carriers of Duchenne and Becker muscular dystrophy in Wales;Clinical Genetics;2008-06-28

4. Molecular Genetics of Duchenne and Becker Muscular Dystrophy;International Review of Neurobiology;1988

5. The molecular genetics of diabetes mellitus;Bioscience Reports;1986-06-01