Carrier Diagnosis of Duchenne Muscular Dystrophy Using Fluorescent CA Repeat Polymorphism
Author:
Publisher
Wiley
Subject
Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1741-4520.1997.tb00978.x/fullpdf
Reference18 articles.
1. Accurate assessment of intra-genic recombination frequency within the Duchenne muscular dystrophy gene;Abbes;Genomics.,1990
2. Gene deletion in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection;Asano;Clin. Genet.,1991
3. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction;Beggs;Hum. Genet.,1990a
4. A polymorphic CACA repeat in the 3′ untranslated region of dystro-phin;Beggs;Nucleic Acids Res.,1990b
5. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification;Chamberlain;Nucleic Acids Res.,1988
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