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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.
Cardiology Research and Practice|March 29, 2021
Atrial Arrhythmias in Patients with Severe COVID-19Kai-Yue Han, Qi Qiao, Ye-Qian Zhu, 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.
Clinical Chemistry and Laboratory Medicine|January 19, 2017
CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathyXing-Biao Qiu, Xin-Kai Qu, Ruo-Gu Li, et al.
Human Mutation|September 4, 2013
GATA4 loss-of-function mutations underlie familial tetralogy of fallotYi-Qing Yang, Lara Gharibeh, Ruo-Gu Li, et al.
Biochemical and Biophysical Research Communications|September 18, 2013
GATA4 loss-of-function mutation underlies familial dilated cardiomyopathyRuo-Gu Li, Li Li, Xing-Biao Qiu, et al.
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