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Scientific Reports|January 9, 2016
In situ genetic correction of F8 intron 22 inversion in hemophilia A patient-specific iPSCsYong Wu, Zhiqing Hu, Zhuo Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 5, 2020
[Clinical practice guidelines for Duchenne muscular dystrophy]Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, Hu Tan, Desheng Liang, et al.
Molecular Genetics & Genomic Medicine|September 22, 2020
REDBot: Natural language process methods for clinical copy number variation reporting in prenatal and products of conception diagnosisMengmeng Liu, Yunshan Zhong, Hongqian Liu, et al.
QJM : Monthly Journal of the Association of Physicians|February 21, 2025
Non-invasive prenatal testing for dominant single-gene disorders using targeted next-generation sequencingHongyun Zhang, Jun He, Yanling Teng, et al.
Cancer Gene Therapy|October 23, 2004
A novel fusion suicide gene yeast CDglyTK plays a role in radio-gene therapy of nasopharyngeal carcinomaKun Xia, Desheng Liang, Aifa Tang, et al.
American Journal of Medical Genetics. Part A|March 31, 2016
De novo exonic deletion of KDM6A in a Chinese girl with Kabuki syndrome: A case report and brief literature reviewPu Yang, Hu Tan, Yan Xia, et al.
Development, Growth & Differentiation|April 27, 2018
Generation of reporter hESCs by targeting EGFP at the CD144 locus to facilitate the endothelial differentiationZhiqing Hu, Yong Wu, Miaojin Zhou, et al.
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