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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 9, 2020
[Genetic analysis of 90 families affected with spinal muscular atrophy]Tao Li, Xue Lyu, Poshi Xu, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 9, 2018
[Identification of a novel EXT1 mutation in a pedigree affected with hereditary multiple exostosis]Guiyu Lou, Ke Yang, Litao Qin, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 12, 2017
[Analysis of genetic polymorphisms and mutations of 20 frequently used STR loci among ethnic Hans from Henan]Hongdan Wang, Bing Kang, Yue Gao, et al.Medicine|October 19, 2019
Prenatal echocardiographic classification and prognostic evaluation strategy in fetal pulmonary atresia with intact ventricular septumLin Liu, Hongdan Wang, Cunying Cui, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 15, 2015
[Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome]Dong Wu, Hongdan Wang, Hui Zhang, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 6, 2017
[Prenatal diagnosis and genetic analysis of a fetus with 6q27 microdeletion]Dong Wu, Weili Shi, Hongdan Wang, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|April 13, 2020
A novel mutation within intron 17 of the CUL7 gene results in appearance of premature termination codonLiangjie Guo, Zhanqi Feng, Xiaoye Jin, et al.Scientific Reports|July 25, 2018
Autosomal DIPs for population genetic structure and differentiation analyses of Chinese Xinjiang Kyrgyz ethnic groupYuxin Guo, Chong Chen, Xiaoye Jin, et al.Journal of Molecular Neuroscience : MN|March 27, 2024
Competing Endogenous RNAs Crosstalk in Hippocampus: A Potential Mechanism for Neuronal Developing Defects in Down SyndromeHuiru Zhao, Guiyu Lou, Yupu Shao, et al.Frontiers in Genetics|September 22, 2023
Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel SyndromeQian Zhang, Shuya Yang, Xin Chen, et al.Pageof 11