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BMC Medical Genetics|May 1, 2015
Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancerSiana N Mtatiro, Josephine Mgaya, Tarjinder Singh, et al.Genetics|May 17, 2006
Fine-scale map of encyclopedia of DNA elements regions in the Korean populationYeon-Kyeong Yoo, Xiayi Ke, Sungwoo Hong, et al.Nature|March 22, 2018
De novo mutations in regulatory elements in neurodevelopmental disordersPatrick J Short, Jeremy F McRae, Giuseppe Gallone, et al.Nature Genetics|February 10, 2006
Common deletion polymorphisms in the human genomeSteven A McCarroll, Tracy N Hadnott, George H Perry, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 21, 2014
Identification of a variant in KDR associated with serum VEGFR2 and pharmacodynamics of PazopanibMichael L Maitland, Chun-Fang Xu, Yu-Ching Cheng, et al.Plos One|November 6, 2014
Genome wide association study of fetal hemoglobin in sickle cell anemia in TanzaniaSiana Nkya Mtatiro, Tarjinder Singh, Helen Rooks, et al.Nature|July 12, 2002
A first-generation linkage disequilibrium map of human chromosome 22Elisabeth Dawson, Gonçalo R Abecasis, Suzannah Bumpstead, et al.Diabetes|March 10, 2012
Deep resequencing unveils genetic architecture of ADIPOQ and identifies a novel low-frequency variant strongly associated with adiponectin variationLiling L Warren, Li Li, Matthew R Nelson, et al.Heart Asia|June 22, 2016
Genome-wide association analysis and replication of coronary artery disease in South Korea suggests a causal variant common to diverse populationsEun Young Cho, Yangsoo Jang, Eun Soon Shin, et al.European Journal of Human Genetics : EJHG|November 21, 2008
Investigation of the fine structure of European populations with applications to disease association studiesSimon C Heath, Ivo G Gut, Paul Brennan, et al.Pageof 19