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CORC

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A rare mosaic 22q11.2 microdeletion identified in a Chinese family with recurrent fetal conotruncal defects 期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 8
作者:  Sheng, Wei;  Li, Xiaodi;  Sun, Liqun;  Huang, Guoying;  Chen, Weicheng
收藏  |  浏览/下载：18/0  |  提交时间：2019/12/05
Repair of Adult Mammalian Heart After Damages by Oral Intake of Gu Ben Pei Yuan San 期刊论文
FRONTIERS IN PHYSIOLOGY, 2019, 卷号: 10
作者:  Cui, Baiping;  Zheng, Yufan;  Zhou, Xinyan;  Zhu, Jiaqi;  Zhuang, Jiexian
收藏  |  浏览/下载：30/0  |  提交时间：2019/12/05
DNA methylation status of TBX20 in patients with tetralogy of Fallot 期刊论文
BMC MEDICAL GENOMICS, 2019, 卷号: 12
作者:  Gong, Juan;  Sheng, Wei;  Ma, Duan;  Huang, Guoying;  Liu, Fang
收藏  |  浏览/下载：6/0  |  提交时间：2019/12/05
Cardiomyocyte orientation modulated by the Numb family proteins-N-cadherin axis is essential for ventricular wall morphogenesis 期刊论文
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 卷号: 116, 期号: 31
作者:  Schwarz, John J.;  Vincent, Peter A.;  Zhong, Weimin;  Radice, Glenn L.;  Wan, Leo Q.
收藏  |  浏览/下载：39/0  |  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：34/0  |  提交时间：2019/12/05
Characteristics and Workload of Pediatricians in China 期刊论文
PEDIATRICS, 2019, 卷号: 144, 期号: 1
作者:  Zhang, Yongjun;  Huang, Lisu;  Zhou, Xin;  Zhang, Xi;  Ke, Zheng
收藏  |  浏览/下载：56/0  |  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
Current practice and awareness of pediatric off-label drug use in Shanghai, China -a questionnaire-based study 期刊论文
BMC PEDIATRICS, 2019, 卷号: 19, 期号: 1
作者:  Mei, Mei;  Xu, Hong;  Wang, Libo;  Huang, Guoying;  Gui, Yonghao
收藏  |  浏览/下载：15/0  |  提交时间：2019/12/05
Novel homozygous ataxia-telangiectasia (A-T) mutated gene mutation identified in a Chinese pedigree with A-T 期刊论文
MOLECULAR MEDICINE REPORTS, 2019, 卷号: 20, 期号: 2
作者:  Hu, Huifang;  Chen, Weicheng;  Liu, Sida;  Chen, Gang;  Zhu, Shaicheng
收藏  |  浏览/下载：28/0  |  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

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