1. Cover. Issue 1 (23rd January 2020) Authors: Lin, Mao; Liu, Zhenlei; Liu, Gang; Zhao, Sen; Li, Chao; Chen, Weisheng; Coban Akdemir, Zeynep; Lin, Jiachen; Song, Xiaofei; Wang, Shengru; Xu, Qiming; Zhao, Yanxue; Wang, Lianlei; Zhang, Yuanqiang; Yan, Zihui; Liu, Sen; Liu, Jiaqi; Chen, Yixin; Zuo, Yuzhi; Yang, Xu Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 1(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1. Issue 1 (27th November 2019) Authors: Lin, Mao; Liu, Zhenlei; Liu, Gang; Zhao, Sen; Li, Chao; Chen, Weisheng; Coban Akdemir, Zeynep; Lin, Jiachen; Song, Xiaofei; Wang, Shengru; Xu, Qiming; Zhao, Yanxue; Wang, Lianlei; Zhang, Yuanqiang; Yan, Zihui; Liu, Sen; Liu, Jiaqi; Chen, Yixin; Zuo, Yuzhi; Yang, Xu Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 1(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Use of medical exome sequencing for identification of underlying genetic defects in NICU: Experience in a cohort of 2303 neonates in China. Issue 1 (25th October 2021) Authors: Yang, Lin; Wei, Zejun; Chen, Xiang; Hu, Liyuan; Peng, Xiaomin; Wang, Jin; Lu, Chunmei; Kong, Yanting; Dong, Xinran; Ni, Qi; Lu, Yulan; Wu, Bingbing; Wang, Huijun; Meirelles, Katia; Tian, Xia; Zhang, Jing; Chang, Fengqi; Liu, Liu; Li, Changhua; You, Wesley Journal: Clinical genetics Issue: Volume 101:Issue 1(2022) Page Start: 101 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗