1. Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome. Issue 1 (21st October 2019) Authors: Boone, Philip M.; Paterson, Scott; Mohajeri, Kiana; Zhu, Wenmiao; Genetti, Casie A.; Tai, Derek J. C.; Nori, Neeharika; Agrawal, Pankaj B.; Bacino, Carlos A.; Bi, Weimin; Talkowski, Michael E.; Hogan, Benjamin M.; Rodan, Lance H. Journal: American journal of medical genetics Issue: Volume 182:Issue 1(2020) Page Start: 189 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗