Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis. - Abstract - Europe PMC
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PDF) Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene
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Figure 5 from Spectrum of mutations in Duchenne Muscular Dystrophy (DMD) and clinical phenotype correlation in Sri Lankan population. | Semantic Scholar
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