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Ophthalmic Genetics|June 28, 2018
A novel MIP mutation in a Chinese family with congenital cataractChao Yuan, Tiantian Han, Pan Su, et al.Human Genetics|August 7, 2024
GBF1 deficiency causes cataracts in human and mouseWeimin Jia, Chenming Zhang, Yalin Luo, et al.Andrology|August 14, 2020
Tsga10 is essential for arrangement of mitochondrial sheath and male fertility in miceGeng Luo, Meiqi Hou, Bo Wang, et al.Reproductive Sciences (Thousand Oaks, Calif.)|June 7, 2022
Novel Compound Heterozygous Mutation in FSIP2 Causes Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) and Male InfertilityMeiqi Hou, Qingsong Xi, Lixia Zhu, et al.Journal of Assisted Reproduction and Genetics|November 3, 2020
A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formationDazhi Zhang, Lixia Zhu, Zhenxing Liu, et al.Reproductive Sciences (Thousand Oaks, Calif.)|May 20, 2022
Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female InfertilityMeiqi Hou, Lixia Zhu, Jinghang Jiang, et al.Plos One|April 19, 2019
Three novel compound heterozygous IL12RB1 mutations in Chinese patients with Mendelian susceptibility to mycobacterial diseaseXiaopei Zhou, Weimin Jia, Zhengyi Ni, et al.Molecular Genetics and Genomics : MGG|December 27, 2022
A novel homozygous mutation in ACTL7A leads to male infertilityXiaopei Zhou, Qingsong Xi, Weimin Jia, et al.Human Genetics|February 6, 2020
Deficiency of SCAMP5 leads to pediatric epilepsy and dysregulation of neurotransmitter release in the brainDazhi Zhang, Chao Yuan, Mengxue Liu, et al.Pageof 2