1. Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly. Issue 1 (December 2016) Authors: Guo, Xingping; Song, Chunying; Shi, Yaping; Li, Hongxia; Meng, Weijing; Yuan, Qinzhao; Xue, Jinjie; Xie, Jun; Liang, Yunxia; Yuan, Yanan; Yu, Baofeng; Wang, Huaixiu; Chen, Yun; Qi, Lixin; Li, Xinmin Journal: BMC medical genetics Issue: Volume 17:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗