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Nature Communications|July 21, 2026
Coverage engineering by shell-number-controlled nanoconfinement enables nitric oxide electroreduction in the ppm regimeShanyuhan Jin, Daliang Xu, Peiwen Xu, et al.Human Genetics|November 9, 2022
Variations in mitochondrial DNA coding and D-loop region are associated with early embryonic development defects in infertile womenYuqing Liu, Shuai Zhao, Xiaolei Chen, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 14, 2018
[Application of droplet digital PCR for non-invasive prenatal diagnosis of single gene disease in two families]Peiwen Xu, Yang Zou, Jie Li, et al.Angewandte Chemie (International Ed. in English)|July 23, 2024
Formulating Self-Repairing Solid Electrolyte Interface via Dynamic Electric Double Layer for Practical Zinc Ion BatteriesSiqi Qin, Jie Zhang, Mi Xu, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 5, 2017
[A novel mutation of GLI3 gene underlying synpolydactyly in a family]Ranran Kang, Sexin Huang, Jie Li, et al.Genes|June 26, 2026
Establishment of a New-Generation National Reference Material System for Fragile X Syndrome Using Targeted Long-Read SequencingMi Zhang, Wenxin Zhang, Fei Gao, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 4, 2020
[Identification of a novel splicing variant of IDS gene in a pedigree affected with type II glycosaminoglycan product storage disease]Hongqiang Xie, Lijuan Wang, Sexin Huang, et al.Clinical Kidney Journal|January 13, 2025
Preimplantation genetic testing for monogenic disorders (PGT-M) for monogenic nephropathy: a single-center retrospective cohort analysisXinyu Liu, Qian Zhang, Kexin Cao, et al.Frontiers in Immunology|January 23, 2024
Low-dose radiotherapy promotes the formation of tertiary lymphoid structures in lung adenocarcinomaDuo Wang, Liuying Huang, Danqi Qian, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 8, 2020
[Identification of a novel variant of COL4A5 gene in a pedigree affected with Alport syndrome]Xiaowei Liu, Ming Gao, Yang Zou, et al.Pageof 5