Identification of copy number variations (CNVs) in a cohort of children and adoles...
Characterization of INDELs and small CNVs in patients with autism spectrum disorder
A statistical method for detection of copy number variation using next-generation ...
Impact of genetic variants on genomic stability and their effects on the phenotype
SNP Arrays data bank analysis of patients with malformations and delay in neuropsy...
CNVs/InDels analysis based on exome data in the etiology of ASD