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Development of Digital Fetal Heart Models with Virtual Ultrasound Function Based on Cardiovascular Casting and Computed Tomography Scan 期刊论文
BIOENGINEERING-BASEL, 2022, 卷号: 9, 期号: 10, 页码: 9
作者:  Yang, Qi;  Han, Jiancheng;  Wang, Rui;  Zhang, Tong;  Zhang, Yingying
收藏  |  浏览/下载:16/0  |  提交时间:2022/11/21
Smyd1 is essential for myosin expression and sarcomere organization in craniofacial, extraocular, and cardiac muscles 期刊论文
JOURNAL OF GENETICS AND GENOMICS, 2021, 卷号: 48, 期号: 3, 页码: 208-218
作者:  Jiao, Shuang;  Xu, Rui;  Du, Shaojun
收藏  |  浏览/下载:16/0  |  提交时间:2021/09/18
Analysis of NKX2-5 in 439 Chinese Patients with Sporadic Atrial Septal Defect 期刊论文
MEDICAL SCIENCE MONITOR, 2019, 卷号: 25
作者:  Wang, Hongshu;  Liu, Yong;  Li, Yaxiong;  Wang, Wenju;  Li, Lin
收藏  |  浏览/下载:28/0  |  提交时间:2019/12/04
Bilateral absence of the superior vena cava presenting with superior vena cava syndrome: A case report 期刊论文
ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES, 2019, 卷号: 36, 期号: 8
作者:  Zhang, Luni;  Zhang, Li;  Wang, Hui;  Chen, Libo
收藏  |  浏览/下载:24/0  |  提交时间:2019/12/05
Insights Figure for "Susceptibility to congenital heart defects associated with a polymorphism in TBX2 3 ' untranslated region in the Han Chinese population'' 期刊论文
PEDIATRIC RESEARCH, 2019, 卷号: 85, 期号: 3
作者:  Wang, Feng
收藏  |  浏览/下载:12/0  |  提交时间:2019/12/05
Susceptibility to congenital heart defects associated with a polymorphism in TBX2 3 ' untranslated region in the Han Chinese population 期刊论文
PEDIATRIC RESEARCH, 2019, 卷号: 85, 期号: 3
作者:  Wang, Jie;  Zhang, Ran-ran;  Ca, Ke;  Yang, Qian;  Duan, Wen-yuan
收藏  |  浏览/下载:2/0  |  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
Intracardiac echogenic focus and its location: association with congenital heart defects. 期刊论文
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2019, 页码: 1-5
作者:  Chiu Gin;  Zhao Andi;  Zhang Bo;  Zhang Tianxiao
收藏  |  浏览/下载:116/0  |  提交时间:2019/11/19
Deficiency of NONO is associated with impaired cardiac function and fibrosis in mice 期刊论文
Journal of Molecular and Cellular Cardiology, 2019, 卷号: 137, 页码: 46-58
作者:  Xu X.;  Jiang H.;  Lu Y.;  Zhang M.;  Cheng C.
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/11
Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype 期刊论文
JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2019, 卷号: Vol.33 No.1
作者:  Song, Tingting;  Wan, Shanning;  Li, Yu;  Xu, Ying;  Dang, Yinghui
收藏  |  浏览/下载:40/0  |  提交时间:2019/12/17


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