Associated Papers
Pitfalls of Multiple Ligation-Dependent Probe Amplifications in Detecting DMD Exon Deletions or Duplications.
Kim MJ et al.
The Journal of Molecular Diagnostics : Jmd, 2016
Genetic diagnosis of Duchenne and Becker muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform.
Lim BC et al.
Journal of Medical Genetics, 2011
Dystrophin point mutation screening using a multiplexed protein truncation test.
Whittock NV et al.
Genetic Testing, 1997
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