PRENATAL TESTING FOR DUCHENNE AND BECKER MUSCULAR DYSTROPHY
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference32 articles.
1. Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences;Kingston;Hum Genet,1984
2. DNA deletions in mild and severe Becker muscular dystrophy;Hart;Hum Genet,1987
3. Oxford monographs on medical genetics no 15: Duchenne muscular dystrophy;Emery,1987
4. The application of linkage analysis to generic counselling in families with Duchenne or Becker muscular dystrophy;Hodgson;J Med Genet,1987
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1. Molecular deletions in the Duchenne/Becker muscular dystrophy gene;Clinical Genetics;2008-06-28
2. Prenatal diagnosis;Journal of Chemical Technology & Biotechnology;2007-04-24
3. Service provision of complex mutation analysis: a technical and economic appraisal using dystrophin point mutation analysis as an example;Clinical Genetics;2002-07
4. 6 Dystrophin, Its Gene, and the Dystrophinopathies;Advances in Genetics;1995
5. Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia;Prenatal Diagnosis;1993-05
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