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(1 - 6 of 6)
Phenotype predictions for exon deletions/duplications: A user guide for professionals and clinicians using Becker and Duchenne muscular dystrophy as examples
Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paraganglioma
Central 22q11.2 Deletions
Hypomorphic NOTCH3 Alleles Do Not Cause CADASIL in Humans
Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature
Subtelomeric Deletion of Chromosome 10p15.3: Clinical Findings and Molecular Cytogenetic Characterization