Association of angiotensin-converting enzyme gene I/D and CYP11B2 gene −344T/C polymorphisms with lone atrial fibrillation and its recurrence after catheter ablation

por ZHANG, XIAN-LING, WU, LI-QUN, LIU, XU, YANG, YI-QING, TAN, HONG-WEI, WANG, XIN-HUA, ZHOU, LI, JIANG, WEI-FENG, LI, ZHENG
Publicado 2012

MEF2C loss-of-function mutation contributes to congenital heart defects

por Qiao, Xiao-Hui, Wang, Fei, Zhang, Xian-Ling, Huang, Ri-Tai, Xue, Song, Wang, Juan, Qiu, Xing-Biao, Liu, Xing-Yuan, Yang, Yi-Qing
Publicado 2017

PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome

por Zhao, Cui-Mei, Peng, Lu-Ying, Li, Li, Liu, Xing-Yuan, Wang, Juan, Zhang, Xian-Ling, Yuan, Fang, Li, Ruo-Gu, Qiu, Xing-Biao, Yang, Yi-Qing
Publicado 2015