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JAMA|March 8, 2017
Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery DiseaseAmit V Khera, Hong-Hee Won, Gina M Peloso, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.
Nature Genetics|February 18, 2025
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 22, 2015
Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defectLisa C A D'Alessandro, Saeed Al Turki, Ashok Kumar Manickaraj, et al.
Cells|March 11, 2023
Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in ACTN2Sophie Broadway-Stringer, He Jiang, Kirsty Wadmore, et al.
Journal of Hypertension|June 14, 2008
Glutathione S-transferase variants and hypertensionChristian Delles, Sandosh Padmanabhan, Wai Kwong Lee, et al.
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