1. Novel de novo 2q14.3 deletion disrupting CNTNAP5 in a girl with intellectual impairment, thin corpus callosum, and microcephaly. Issue 7 (24th April 2020) Authors: Ludington, Eleanor G.; Yu, Sui; Bae, Ha Ae; Barnett, Christopher P. Journal: American journal of medical genetics Issue: Volume 182:Issue 7(2020) Page Start: 1824 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗