1. Gain‐of‐function mutations in SMAD4 cause a distinctive repertoire of cardiovascular phenotypes in patients with Myhre syndrome. Issue 10 (14th June 2016) Authors: Lin, Angela E.; Michot, Caroline; Cormier‐Daire, Valerie; L'Ecuyer, Thomas J.; Matherne, G. Paul; Barnes, Barrett H.; Humberson, Jennifer B.; Edmondson, Andrew C.; Zackai, Elaine; O'Connor, Matthew J.; Kaplan, Julie D.; Ebeid, Makram R.; Krier, Joel; Krieg, Elizabeth; Ghoshhajra, Brian; Lindsay, ... Other Names: Hennekam Raoul C.M. guestEditor.; Biesecker Leslie G. guestEditor. Journal: American journal of medical genetics Issue: Volume 170:Issue 10(2016) Page Start: 2617 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗