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Journal of Medical Genetics|June 15, 2007
Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertensionAna Carolina Braga Marçano, Beverley Burke, Johannie Gungadoo, et al.
Circulation. Genomic and Precision Medicine|March 13, 2020
Reevaluation of the South Asian MYBPC3Δ25bp Intronic Deletion in Hypertrophic CardiomyopathyAndrew R Harper, Michael Bowman, Jesse B G Hayesmoore, et al.
Annals of Human Genetics|July 30, 2014
Global genetic architecture of an erythroid quantitative trait locus, HMIP-2Stephan Menzel, Helen Rooks, Diana Zelenika, et al.
Lancet (London, England)|June 27, 2003
Genome-wide mapping of human loci for essential hypertensionMark Caulfield, Patricia Munroe, Janine Pembroke, et al.
Journal of Hypertension|June 14, 2008
Glutathione S-transferase variants and hypertensionChristian Delles, Sandosh Padmanabhan, Wai Kwong Lee, et al.
Nature Genetics|December 17, 2013
Meta-analysis of gene-level tests for rare variant associationDajiang J Liu, Gina M Peloso, Xiaowei Zhan, et al.
Hypertension (Dallas, Tex. : 1979)|November 1, 2006
Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiencyMarianne Barr, Scott M MacKenzie, Elaine C Friel, et al.
Hypertension (Dallas, Tex. : 1979)|June 7, 2006
Increased support for linkage of a novel locus on chromosome 5q13 for essential hypertension in the British Genetics of Hypertension StudyPatricia B Munroe, Chris Wallace, Ming-Zhan Xue, et al.
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