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Journal of Human Genetics|October 24, 2000
Multiplex PCR amplification of TH01, D9S304, and D3S1744 lociK Fujii, H Senju, K Yoshida, et al.Journal of Human Genetics|October 24, 2000
cDNA cloning of a human RAB26-related gene encoding a Ras-like GTP-binding protein on chromosome 16p13.3 regionN Seki, T Yoshikawa, A Hattori, et al.Journal of Human Genetics|April 3, 2001
Amino-acid substitutions in the IKAP gene product significantly increase risk for bronchial asthma in childrenS Takeoka, M Unoki, Y Onouchi, et al.Journal of Human Genetics|November 22, 2017
Application of genome editing technologies in rats for human disease modelsKazuto Yoshimi, Tomoji MashimoJournal of Human Genetics|November 24, 2017
Updated summary of genome editing technology in human cultured cells linked to human genetics studiesTatsuo Miyamoto, Silvia Natsuko Akutsu, Shinya MatsuuraJournal of Human Genetics|November 24, 2017
Phenotypic expression of a novel desmin gene mutation: hypertrophic cardiomyopathy followed by systemic myopathyHaruhito Harada, Takeharu Hayashi, Hirofumi Nishi, et al.Journal of Human Genetics|March 2, 2018
Integrative functional analysis of super enhancer SNPs for coronary artery diseaseJuexiao Gong, Chuan Qiu, Dan Huang, et al.Journal of Human Genetics|December 4, 2018
Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversusWeizhi Zhang, Dongping Li, Shijie Wei, et al.Journal of Human Genetics|March 22, 2018
Association of a single nucleotide polymorphism in TNIP1 with type-1 autoimmune hepatitis in the Japanese populationShomi Oka, Takashi Higuchi, Hiroshi Furukawa, et al.Journal of Human Genetics|March 22, 2018
A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese familyYuyuan Deng, Zhijie Niu, LiangLiang Fan, et al.Pageof 352