Implications of a common polymorphism in intron 12 of the dystrophin gene for deletion detection by multiplex PCR
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference28 articles.
1. A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods;Abbs;J. Med. Genet.,1991
2. Statement on storage and use of genetic materials;Am. J. Hum. Genet.,1995
3. A nonsense mutation (Gln-673-Term) in exon 17 of the human dystrophin gene detected by heteroduplex analysis;Barbieri;Hum. Genet.,1995
4. A novel splice site mutation in a Becker muscular dystrophy patient;Bartolo;J. Med. Genet.,1996
5. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction;Beggs;Hum. Genet.,1990
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4. Detection and identification of base alterations within the region of factor V leiden by fluorescent melting curves*;Molecular Diagnosis;1998-12
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