Multiplex PCR for Identifying Dystrophin Gene Deletions
Author:
Affiliation:
1. Children's Hospital and Harvard Medical School Boston Massachusetts
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142905.hg0903s10
Reference40 articles.
1. Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene.
2. A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods.
3. Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses.
4. Exploring the molecular basis for variability among patients with Becker muscular dystrophy: Dystrophin gene and protein studies;Beggs A.H.;Am. J. Hum. Genet.,1991
5. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
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1. FSHD-like patients without 4q35 deletion;Journal of the Neurological Sciences;2004-04
2. Duchenne and Becker muscular dystrophies: an Estonian experience;Brain and Development;1999-06
3. Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization;Neuromuscular Disorders;1998-10
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