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Journal of Human Genetics|November 11, 2011
Genetic variations in the CYP17A1 and NT5C2 genes are associated with a reduction in visceral and subcutaneous fat areas in Japanese womenKikuko Hotta, Aya Kitamoto, Takuya Kitamoto, et al.Journal of Human Genetics|February 16, 2006
Fifty years of genetic epidemiology, with special reference to JapanNewton E MortonJournal of Human Genetics|December 22, 2007
A meta-analysis of DNA repair gene XPC polymorphisms and cancer riskDeqiang Zhang, Chengwen Chen, Xuping Fu, et al.Journal of Human Genetics|February 4, 1999
Novel germline mutations of the MEN1 gene in Japanese patients with multiple endocrine neoplasia type 1K Hamaguchi, D C Nguyen, T Yanase, et al.Journal of Human Genetics|February 4, 1999
Localization of human midisatellite and macrosatellite DNA sequences on chromosomes 1 and X in the great apesR V Samonte, R A Conte, R S VermaJournal of Human Genetics|February 4, 1999
Another observation of microphthalmia in an XX male: microphthalmia with linear skin defects syndrome without linear skin lesionsT Kono, T Migita, S Koyama, et al.Journal of Human Genetics|November 11, 2016
Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5'UTR and founder alleleWenhua Zhu, Satomi Mitsuhashi, Takahiro Yonekawa, et al.Journal of Human Genetics|November 11, 2016
Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasiaLong Guo, Katta M Girisha, Aritoshi Iida, et al.Journal of Human Genetics|January 6, 2017
Comprehensive genotyping in dyslipidemia: mendelian dyslipidemias caused by rare variants and Mendelian randomization studies using common variantsHayato Tada, Masa-Aki Kawashiri, Masakazu YamagishiJournal of Human Genetics|May 3, 2014
Very early-onset inflammatory bowel disease (IBD) in infancy is a different disease entity from adult-onset IBD; one form of interleukin-10 receptor mutationsJung Ok Shim, Jeong Kee SeoPageof 352