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Cell Discovery|August 2, 2017
A TBX5 3'UTR variant increases the risk of congenital heart disease in the Han Chinese populationFeng Wang, Dong Liu, Ran-Ran Zhang, et al.
Journal of Cellular and Molecular Medicine|July 5, 2022
PARD3 gene variation as candidate cause of nonsyndromic cleft palate onlyRenjie Cui, Dingli Chen, Na Li, et al.
Asian Journal of Andrology|June 15, 2010
The role of Dby mRNA in early development of male mouse zygotesChen-Jiang Yao, Wang-Jie Xu, Xiu-Li Gong, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 5, 2020
[A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (4) - Report interpretation and genetic counseling]Hui Huang, Yiping Shen, Weihong Gu, et al.
Clinical and Translational Medicine|July 9, 2022
WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferationLili Hao, Jing Ma, Feizhen Wu, et al.
Clinical and Translational Medicine|July 13, 2024
A hidden proteome encoded by circRNAs in human placentas: Implications for uncovering preeclampsia pathogenesisHuanqiang Zhao, Yu Xiong, Zixiang Zhou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 5, 2020
[A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (1) - Procedures prior to genetic testing]Jian Wang, Weihong Gu, Hui Huang, et al.
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