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Journal of Medical Genetics|March 31, 2006
Functional and clinical characterization of a mutation in KCNJ2 associated with Andersen-Tawil syndromeC-W Lu, J-H Lin, Y S Rajawat, et al.
Journal of the National Cancer Institute|November 12, 2023
Dyslipidemia and cardiovascular disease among childhood cancer survivors: a St. Jude Lifetime Cohort reportJason F Goldberg, Geehong Hyun, Kirsten K Ness, et al.
Journal of the American College of Cardiology|November 25, 2017
Survival Without Cardiac Transplantation Among Children With Dilated CardiomyopathyRakesh K Singh, Charles E Canter, Ling Shi, et al.
Heart Rhythm|June 7, 2008
Risk of death in the long QT syndrome when a sibling has diedElizabeth S Kaufman, Scott McNitt, Arthur J Moss, et al.
American Journal of Medical Genetics. Part A|April 4, 2003
Toward a genetic etiology of CHARGE syndrome: I. A systematic scan for submicroscopic deletionsSeema R Lalani, David W Stockton, Carlos Bacino, et al.
Circulation|April 19, 2006
Beta2-adrenergic receptor genetic variants and risk of sudden cardiac deathNona Sotoodehnia, David S Siscovick, Matteo Vatta, et al.
Molecular Genetics and Metabolism|June 26, 2009
Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephalyErich Roessler, Wuhong Pei, Maia V Ouspenskaia, et al.
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