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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.Journal of Human Genetics|September 8, 2017
The pharmacogenomics of valproic acidMiao-Miao Zhu, Hui-Lan Li, Li-Hong Shi, et al.Journal of Human Genetics|March 18, 2016
Spectrum of AGL mutations in Chinese patients with glycogen storage disease type III: identification of 31 novel mutationsChaoxia Lu, Zhengqing Qiu, Miao Sun, et al.Journal of Human Genetics|December 4, 2015
An epigenomic signature of postprandial hyperglycemia in peripheral blood leukocytesSung-Mi Shim, Yoon-Kyung Cho, Eun-Jung Hong, et al.Journal of Human Genetics|December 4, 2015
The African-387 C>T TGFB1 variant is functional and associates with the ophthalmoplegic complication in juvenile myasthenia gravisMelissa Nel, Joy-Mari Buys, Robyn Rautenbach, et al.Journal of Human Genetics|October 26, 2017
The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effectsVittoria Trezzi, Diego Forni, Roberto Giorda, et al.Journal of Human Genetics|September 15, 2017
Skewed X inactivation in Lesch-Nyhan disease carrier femalesRosa J Torres, Juan G PuigJournal of Human Genetics|September 28, 2019
Long-read sequencing for rare human genetic diseasesSatomi Mitsuhashi, Naomichi MatsumotoPageof 351