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Journal of Molecular Histology|December 7, 2017
Restoration of SMN expression in mesenchymal stem cells derived from gene-targeted patient-specific iPSCsMai Feng, Cong Liu, Yan Xia, et al.Muscle & Nerve|December 20, 2014
PMP22-Related neuropathies and other clinical manifestations in Chinese han patients with charcot-marie-tooth disease type 1Yajing Zhan, Xiaohong Zi, Zhengmao Hu, et al.International Journal of Molecular Sciences|October 11, 2018
Paired CRISPR/Cas9 Nickases Mediate Efficient Site-Specific Integration of <i>F9</i> into rDNA Locus of Mouse ESCsYanchi Wang, Junya Zhao, Nannan Duan, et al.Reproduction (Cambridge, England)|January 31, 2016
Chromosomal analysis of blastocysts from balanced chromosomal rearrangement carriersBaoheng Gui, Zhongyuan Yao, Yanping Li, et al.Acta Biochimica Et Biophysica Sinica|December 17, 2009
A non-viral vector for potential DMD gene therapy study by targeting a minidystrophin-GFP fusion gene into the hrDNA locusJunlin Yang, Xionghao Liu, Jiaoling Yu, et al.Gene|April 4, 2015
Novel de novo nonsense mutation of the PHEX gene (p.Lys50Ter) in a Chinese patient with hypophosphatemic ricketsYanru Huang, Libin Mei, Qian Pan, et al.Journal of Medical Genetics|July 26, 2018
XRCC2 mutation causes meiotic arrest, azoospermia and infertilityYongjia Yang, Jihong Guo, Lei Dai, et al.Molecular Cytogenetics|March 17, 2015
Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosomeRuiyu Ma, Ying Peng, Yanghui Zhang, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|November 20, 2016
Targeted exome sequencing identifies novel compound heterozygous mutations in P3H1 in a fetus with osteogenesis imperfecta type VIIIYanru Huang, Libin Mei, Weigang Lv, et al.The Journal of Molecular Diagnostics : JMD|July 8, 2014
Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromesDesheng Liang, Ying Peng, Weigang Lv, et al.Pageof 20