Showing results (151-160 of 194) with videos related to
Sort By:
Pageof 20
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.Plos One|May 23, 2012
Targeting of the human coagulation factor IX gene at rDNA locus of human embryonic stem cellsXionghao Liu, Yong Wu, Zhuo Li, 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.Prenatal Diagnosis|March 7, 2026
Low-Pass Genome Sequencing Reveals Associations Between Chromosomal Aberrations and Ultrasonographic Anomalies in a Cohort of 19,452 FetusesLijuan Pan, Jiayu Wu, Yi Zhang, 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.Human Gene Therapy|March 31, 2018
Seamless Genetic Conversion of SMN2 to SMN1 via CRISPR/Cpf1 and Single-Stranded Oligodeoxynucleotides in Spinal Muscular Atrophy Patient-Specific Induced Pluripotent Stem CellsMiaojin Zhou, Zhiqing Hu, Liyan Qiu, et al.Pageof 20