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Paper Details

Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.
PLoS One
50
2013
185 CNVs, ASD, ASD-associated CNVs, ASDs, CNVs, SNP array, SNV probes, SNVs, autism, autism spectrum disorders, autism-specific CNVs, children, copy number variants, custom Illumina array, custom array, human, single nucleotide variants
Author NameAffiliation
Nori MatsunamiUniversity of Utah
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Datasets

Release 1.2