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Journal of Human Genetics|September 26, 2014
KIF1A mutation in a patient with progressive neurodegenerationNobuhiko Okamoto, Fuyuki Miya, Tatsuhiko Tsunoda, et al.Journal of Human Genetics|May 31, 2013
Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disordersHidenobu Soejima, Ken HigashimotoJournal of Human Genetics|May 3, 2013
Pharmacogenomics of endocrine therapy in breast cancerJames N IngleJournal of Human Genetics|June 14, 2013
Molecular pathology of Sandhoff disease with p.Arg505Gln in HEXB: application of simulation analysisNaoko Yasui, Yutaka Takaoka, Hisahide Nishio, et al.Journal of Human Genetics|June 7, 2013
Effects of embryonic manipulation and epigeneticsTakashi KohdaJournal of Human Genetics|November 1, 2013
A genome-wide association study of third molar agenesis in Japanese and Korean populationsShugo Haga, Hirofumi Nakaoka, Tetsutaro Yamaguchi, et al.Journal of Human Genetics|September 27, 2013
Clinical features and management of organic acidemias in JapanDaisuke Fujisawa, Kimitoshi Nakamura, Hiroshi Mitsubuchi, et al.Journal of Human Genetics|July 12, 2013
Complete genome sequencing and variant analysis of a Pakistani individualMuhammad Kamran Azim, Chuanchun Yang, Zhixiang Yan, et al.Journal of Human Genetics|February 24, 2012
Family history of von Hippel-Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patientsPengjie Wu, Ning Zhang, Xi Wang, et al.Journal of Human Genetics|March 2, 2012
Impact of common type 2 diabetes risk gene variants on future type 2 diabetes in the non-diabetic population in KoreaSe Eun Park, Won Young Lee, Ki Won Oh, et al.Pageof 351