Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1990.tb03500.x/fullpdf
Reference34 articles.
1. Germline mosaidsm and Duchenne muscular dystrophy mutations;Bakker;Nature,1987
2. Regional mapping of coagulation factor IX gene and several unique DNA sequences of the human X chromosome;Camerino;Cytogenet. Cell Genet.,1984
3. A genetic linkage map of five marker loci in and around the muscular dystrophy locus;Chen;Genomics,1989
4. Prenatal diagnosis and detection of carriers with DNA probes in Duchenne muscular dystrophy;Darras;N. Engl. J. Med.,1987
5. A partial deletion of a muscular dystrophy gene transmitted twice by an unaffected male;Darras;Nature,1987
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1. Carrier Testing of Children for Two X-Linked Diseases: A Retrospective Study of Comprehension of the Test Results and Social and Psychological Significance of the Testing;Pediatrics;2000-12-01
2. Carrier Testing of Children for Two X-Linked Diseases: A Retrospective Evaluation of Experience and Satisfaction of Subjects and Their Mothers;Genetic Testing;1999-01
3. Muscular dystrophy: Centronucleation may reflect a compensatory activation of defective myonuclei;Journal of Biomedical Science;1998-01
4. 6 Dystrophin, Its Gene, and the Dystrophinopathies;Advances in Genetics;1995
5. Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA;The Lancet;1990-12
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