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European Journal of Medical Genetics|September 8, 2014
Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart diseaseLan Zhao, Shi-Hong Ni, Xing-Yuan Liu, et al.
International Journal of Medical Sciences|May 30, 2017
TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosusRi-Tai Huang, Juan Wang, Song Xue, et al.
European Journal of Medical Genetics|December 10, 2017
A novel NR2F2 loss-of-function mutation predisposes to congenital heart defectXiao-Hui Qiao, Qian Wang, Juan Wang, et al.
The American Journal of Cardiology|December 3, 2014
A novel NKX2.5 loss-of-function mutation associated with congenital bicuspid aortic valveXin-Kai Qu, Xing-Biao Qiu, Fang Yuan, et al.
Biochemical and Biophysical Research Communications|March 1, 2015
TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathyXian-Ling Zhang, Xing-Biao Qiu, Fang Yuan, et al.
Lung Cancer (Amsterdam, Netherlands)|August 26, 2017
Validation of ALK/ROS1 Dual Break Apart FISH Probe probe in non-small-cell lung cancerSun Min Lim, Hyun Chang, Yoon Jin Cha, et al.
Heart and Vessels|February 16, 2018
ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathyYu-Min Sun, Jun Wang, Ying-Jia Xu, et al.
The Canadian Journal of Cardiology|January 20, 2023
T-Cell Mineralocorticoid Receptor Deficiency Attenuates Pathologic Ventricular Remodelling After Myocardial InfarctionYong-Li Wang, Xiao-Xin Ma, Ruo-Gu Li, et al.
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