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Annals of Human Genetics|December 17, 2019
DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagellaYanwei Sha, Xiaoli Wei, Lu Ding, et al.Frontiers in Genetics|October 30, 2024
Preimplantation genetic testing for Cockayne syndrome with a novel ERCC6 variant in a Chinese familyXuemei He, Yiyuan Zhang, Xianjing Huang, et al.Journal of Human Genetics|June 20, 2020
Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotypeYanwei Sha, Xiaoli Wei, Lu Ding, et al.Frontiers in Medicine|June 1, 2026
Genetic analysis of <i>F8</i> mutations in five hemophilia a carriersHuizi Sun, Libin Mei, Xuemei He, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|March 3, 2019
Exome sequencing identifies compound heterozygous KCTD7 mutations in a girl with progressivemyoclonus epilepsyLibin Mei, Yanru Huang, Jing Chen, et al.Molecular Genetics & Genomic Medicine|July 4, 2019
EIF4G1 is a novel candidate gene associated with severe asthenozoospermiaYanwei Sha, Wensheng Liu, Xianjing Huang, et al.Molecules (Basel, Switzerland)|February 26, 2025
The Production and Characterization of an Aminolyzed Polyhydroxyalkanoate Membrane and Its Cytocompatibility with OsteoblastsQiulan Luo, Fuming Zou, Dongjuan Yang, et al.Clinical Genetics|February 28, 2019
DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagellaYang Li, Yanwei Sha, Xiong Wang, et al.Pageof 2