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Human Genetics|July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisationR M Winter, K E Davies, M V Bell, et al.Human Genetics|July 9, 2016
Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith-Magenis syndrome with evident peripheral neuropathyBo Yuan, Juanita Neira, Shen Gu, et al.Human Genetics|February 23, 2016
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain AtlasElse Eising, Sjoerd M H Huisman, Ahmed Mahfouz, et al.Human Genetics|February 15, 2016
Adaptive evolution of interleukin-3 (IL3), a gene associated with brain volume variation in general human populationsMing Li, Liang Huang, Kaiqin Li, et al.Human Genetics|February 18, 2016
New molecular insights into modulation of platelet reactivity in aspirin-treated patients using a network-based approachAnne Zufferey, Mark Ibberson, Jean-Luc Reny, et al.Human Genetics|December 29, 2014
CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLsMargus Putku, Mart Kals, Rain Inno, et al.Human Genetics|July 30, 2015
Common polygenic variation contributes to risk of migraine in the Norfolk Island populationA J Rodriguez-Acevedo, M A Ferreira, Miles C Benton, et al.Human Genetics|November 14, 2015
Detection of low-prevalence somatic TSC2 mutations in sporadic pulmonary lymphangioleiomyomatosis tissues by deep sequencingAtsushi Fujita, Katsutoshi Ando, Etsuko Kobayashi, et al.Human Genetics|November 9, 2015
Pathway-based variant enrichment analysis on the example of dilated cardiomyopathyChristina Backes, Benjamin Meder, Alan Lai, et al.Human Genetics|November 13, 2015
Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial cleftsFederica Conte, Martin Oti, Jill Dixon, et al.Pageof 958