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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
Accuracy of cardiac auscultation in detection of neonatal congenital heart disease by general paediatricians 期刊论文
CARDIOLOGY IN THE YOUNG, 2019, 卷号: 29, 期号: 5
作者:  Zhao, Qu-ming;  Niu, Conway;  Liu, Fang;  Wu, Lin;  Ma, Xiao-jing
收藏  |  浏览/下载:35/0  |  提交时间:2019/12/05
Functional analysis of the congenital heart disease-associated GATA4 H436Y mutation in vitro 期刊论文
MOLECULAR MEDICINE REPORTS, 2019, 卷号: 20, 期号: 3
作者:  Fang, Tao;  Zhu, Yanjie;  Xu, Anlan;  Zhang, Yanli;  Wu, Qingfa
收藏  |  浏览/下载:33/0  |  提交时间:2019/12/05
DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome 期刊论文
SCIENTIFIC REPORTS, 2019, 卷号: 9
作者:  Liu, Sida;  Chen, Weicheng;  Zhan, Yongkun;  Li, Shuolin;  Ma, Xiaojing
收藏  |  浏览/下载:24/0  |  提交时间:2019/12/05
A regulatory variant in TBX2 promoter is related to the decreased susceptibility of congenital heart disease in the Han Chinese population 期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 2
作者:  Zhang, Ran-ran;  Cai, Ke;  Liu, Lian;  Yang, Qian;  Zhang, Ping
收藏  |  浏览/下载:0/0  |  提交时间:2019/12/05
Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort 期刊论文
JOURNAL OF HUMAN GENETICS, 2019, 卷号: 64, 期号: 5
作者:  Ma, Xiao-Yun;  Ding, Pei-Cheng;  Tang, Han-Fei;  Peng, Rui;  Lu, Lei
收藏  |  浏览/下载:23/0  |  提交时间:2019/12/05
Prevalence of Congenital Heart Disease at Live Birth in China 期刊论文
JOURNAL OF PEDIATRICS, 2019, 卷号: 204
作者:  Zhao, Qu-Ming;  Liu, Fang;  Wu, Lin;  Ma, Xiao-Jing;  Niu, Conway
收藏  |  浏览/下载:8/0  |  提交时间:2019/12/05
Association of functional variant in GDF1 promoter with risk of congenital heart disease and its regulation by Nkx2.5 期刊论文
CLINICAL SCIENCE, 2019, 卷号: 133, 期号: 12
作者:  Gao, Xiaobo;  Zheng, Panpan;  Yang, Liping;  Luo, Haiyan;  Zhang, Chen
收藏  |  浏览/下载:15/0  |  提交时间:2019/12/05
MIB1 mutations reduce Notch signaling activation and contribute to congenital heart disease 期刊论文
CLINICAL SCIENCE, 2018, 卷号: 132, 期号: 23
作者:  Li, Binbin;  Yu, Liwei;  Liu, Dong;  Yang, Xueyan;  Zheng, Yufang
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/05
Current status of screening, diagnosis, and treatment of neonatal congenital heart disease in China 期刊论文
WORLD JOURNAL OF PEDIATRICS, 2018, 卷号: 14, 期号: 4
作者:  Ma, Xiao-Jing;  Huang, Guo-Ying
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/05


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