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Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]|February 9, 2010
[Correlates of bronchial asthma in Uygur and Han adults in Turpan prefecture, Xinjiang]Jing Wang, Man-Gu-Li Wu-Shou-Er Qi, Xia Li, et al.
Zhongguo Zhong Xi Yi Jie He Za Zhi Zhongguo Zhongxiyi Jiehe Zazhi = Chinese Journal of Integrated Traditional and Western Medicine|April 25, 2014
[C825T polymorphism of G protein beta3 subunit gene and Uygur Hilit type of essential hypertension: a correlation study]Xiao-Xi Li, Yu-Nu-Si A-Yi-Gu-Li, Jing-Jing Huang, et al.
International Heart Journal|September 6, 2019
A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right VentricleZhi Wang, Hao-Ming Song, Fei Wang, et al.
European Journal of Medical Genetics|September 16, 2018
HAND2 loss-of-function mutation causes familial dilated cardiomyopathyHua Liu, Ying-Jia Xu, Ruo-Gu Li, et al.
International Journal of Medical Sciences|August 29, 2013
PITX2c loss-of-function mutations responsible for congenital atrial septal defectsFang Yuan, Lan Zhao, Juan Wang, et al.
Heart and Vessels|November 4, 2018
ISL1 loss-of-function mutation contributes to congenital heart defectsLan Ma, Juan Wang, Li Li, et al.
European Journal of Medical Genetics|July 4, 2012
GATA6 loss-of-function mutation in atrial fibrillationYi-Qing Yang, Li Li, Juan Wang, et al.
Molecular Medicine Reports|May 29, 2015
Prevalence and spectrum of LRRC10 mutations associated with idiopathic dilated cardiomyopathyXin-Kai Qu, Fang Yuan, Ruo-Gu Li, et al.
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