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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.
International Journal of Molecular Medicine|February 6, 2019
NR2F2 loss‑of‑function mutation is responsible for congenital bicuspid aortic valveJuan Wang, Pradhan Abhinav, Ying-Jia Xu, et al.
International Journal of Molecular Medicine|August 15, 2014
GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathyLei Xu, Lan Zhao, Fang Yuan, et al.
International Heart Journal|July 10, 2020
A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular BlockYan Zhang, Yu-Min Sun, Ying-Jia Xu, et al.
European Journal of Medical Genetics|August 11, 2020
ISL1 loss-of-function variation causes familial atrial fibrillationShao-Hui Wu, Xin-Hua Wang, Ying-Jia Xu, et al.
Molecular Medicine Reports|March 6, 2017
Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular blockYing-Jia Xu, Xing-Biao Qiu, Fang Yuan, et al.
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