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NR2F2 loss-of-function mutation is responsible for congenital bicuspid aortic valve 期刊论文
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2019, 卷号: 43, 期号: 4
作者:  Wang, Juan;  Abhinav, Pradhan;  Xu, Ying-Jia;  Li, Ruo-Gu;  Zhang, Min
收藏  |  浏览/下载:54/0  |  提交时间:2019/12/05
Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy 期刊论文
JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH, 2019, 卷号: 12, 期号: 3
作者:  Xu, Ying-Jia;  Wang, Zhang-Sheng;  Yang, Chen-Xi;  Di, Ruo-Min;  Qiao, Qi
收藏  |  浏览/下载:79/0  |  提交时间:2019/12/05
ISL1 loss-of-function mutation contributes to congenital heart defects 期刊论文
HEART AND VESSELS, 2019, 卷号: 34, 期号: 4
作者:  Ma, Lan;  Wang, Juan;  Li, Li;  Qiao, Qi;  Di, Ruo-Min
收藏  |  浏览/下载:25/0  |  提交时间:2019/12/05
GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve 期刊论文
GENE, 2018, 卷号: 663
作者:  Xu, Ying-Jia;  Di, Ruo-Min;  Qiao, Qi;  Li, Xiu-Mei;  Huang, Ri-Tai
收藏  |  浏览/下载:18/0  |  提交时间:2019/12/05
A SHOX2 loss-of-function mutation underlying familial atrial fibrillation 期刊论文
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES, 2018, 卷号: 15, 期号: 13
作者:  Li, Ning;  Wang, Zhang-Sheng;  Wang, Xin-Hua;  Xu, Ying-Jia;  Qiao, Qi
收藏  |  浏览/下载:13/0  |  提交时间:2019/12/05
Chinese systemic lupus erythematosus treatment and research group registry IX: Clinical features and survival of childhood-onset systemic lupus erythematosus in china 期刊论文
Chinese Medical Journal, 2017, 卷号: 130, 页码: 1276-1282
作者:  Wu, Chan-Yuan;  Li, Cai-Feng;  Wu, Qing-Jun;  Xu, Jian-Hua;  Jiang, Lin-Di
收藏  |  浏览/下载:56/0  |  提交时间:2019/11/26
Surface Electromagnetic Prospecting System (SEP) contrast test in Caosiyao molybdenum mine, inner mongolia 期刊论文
CHINESE JOURNAL OF GEOPHYSICS-CHINESE EDITION, 2015, 卷号: 58, 期号: 8, 页码: 2654-2663
作者:  Di Qing-Yun;  Xu Cheng;  Fu Chang-Min;  Wang Zhong-Xing;  Zhang Wen-Xiu
收藏  |  浏览/下载:15/0  |  提交时间:2017/12/07


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