1. Deletion 16p13.11 uncovers NDE1 mutations on the non‐deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption. Issue 7 (23rd May 2013) Authors: Paciorkowski, Alex R.; Keppler‐Noreuil, Kim; Robinson, Luther; Sullivan, Christopher; Sajan, Samin; Christian, Susan L.; Bukshpun, Polina; Gabriel, Stacy B.; Gleeson, Joseph G.; Sherr, Elliott H.; Dobyns, William B. Journal: American journal of medical genetics Issue: Volume 161:Issue 7(2013:Jul.) Page Start: 1523 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗