Showing results (1811-1820 of 3,522) with videos related to
Sort By:
Pageof 353
Journal of Human Genetics|May 11, 2012
Evaluating rare variants under two-stage designQizhai Li, Dongdong Pan, Weihua Yue, et al.Journal of Human Genetics|May 18, 2012
High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiencyAlzbeta Vondrackova, Katerina Vesela, Hana Hansikova, et al.Journal of Human Genetics|September 18, 2015
A pilot study of gene testing of genetic bone dysplasia using targeted next-generation sequencingHuiwen Zhang, Rui Yang, Yu Wang, et al.Journal of Human Genetics|May 20, 2016
Reproductive outcomes following preimplantation genetic diagnosis using fluorescence in situ hybridization for 52 translocation carrier couples with a history of recurrent pregnancy lossKeiichi Kato, Naoki Aoyama, Nami Kawasaki, et al.Journal of Human Genetics|May 20, 2016
A significant association between rs8067378 at 17q12 and invasive cervical cancer originally identified by a genome-wide association study in Han Chinese is replicated in a Japanese populationKiyonori Miura, Hiroyuki Mishima, Michio Yasunami, et al.Journal of Human Genetics|April 8, 2016
A PDE3A mutation in familial hypertension and brachydactyly syndromeHiroko Boda, Hidetoshi Uchida, Nobue Takaiso, et al.Journal of Human Genetics|May 13, 2016
Dual-receptor (EGFR and c-MET) inhibition by tumor-suppressive miR-1 and miR-206 in head and neck squamous cell carcinomaKeiichi Koshizuka, Toyoyuki Hanazawa, Ichiro Fukumoto, et al.Journal of Human Genetics|June 10, 2016
Regulation of metastasis-promoting LOXL2 gene expression by antitumor microRNAs in prostate cancerMayuko Kato, Akira Kurozumi, Yusuke Goto, et al.Journal of Human Genetics|August 11, 2017
Population-based biobank participants' preferences for receiving genetic test resultsKayono Yamamoto, Tsuyoshi Hachiya, Akimune Fukushima, et al.Journal of Human Genetics|September 26, 2017
Corrigendum: Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutationsMariko Okubo, Narihiro Minami, Kanako Goto, et al.Pageof 353