1. Bi‐allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalus. Issue 3 (17th January 2018) Authors: Ruggeri, Gaia; Timms, Andrew E.; Cheng, Chi; Weiss, Avery; Kollros, Peter; Chapman, Teresa; Tully, Hannah; Mirzaa, Ghayda M. Journal: American journal of medical genetics Issue: Volume 176:Issue 3(2018) Page Start: 676 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗