PMC:4067558 / 46323-46520 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/4067558","sourcedb":"PMC","sourceid":"4067558","source_url":"https://www.ncbi.nlm.nih.gov/pmc/4067558","text":"(A) Percentage of individuals with CNVs overlapping genes and loci implicated in ASD and/or ID (“all CNV”), pathogenic CNVs, uncertain CNVs, or benign CNVs; and OR in affected and control subjects.","tracks":[]}