1. Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly. (January 2017) Authors: Wang, Bo; Li, Niu; Geng, Juan; Wang, Zhigang; Fu, Qihua; Wang, Jian; Xu, Yunlan Journal: Congenital anomalies Issue: Volume 57:Number 1(2017) Page Start: 4 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗