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Circulation. Cardiovascular Genetics|August 13, 2011
Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndromeDavid J Tester, Bi-Hua Tan, Argelia Medeiros-Domingo, et al.
Heart Rhythm|September 7, 2010
Implantable cardioverter defibrillator therapy for congenital long QT syndrome: a single-center experienceJustin M Horner, Masayoshi Kinoshita, Tracy L Webster, et al.
Mayo Clinic Proceedings|May 8, 2012
Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traitsKeyue Ding, Khader Shameer, Hayan Jouni, et al.
Environmental Health Perspectives|April 5, 2013
Climate change, human health, and biomedical research: analysis of the National Institutes of Health research portfolioChristine M Jessup, John M Balbus, Carole Christian, et al.
Mayo Clinic Proceedings|July 4, 2003
Primer on medical genomics. Part VIII: Essentials of medical genetics for the practicing physicianRegina E Ensenauer, Shanda S Reinke, Michael J Ackerman, et al.
Cardiovascular Research|July 19, 2002
A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletineCarmen R Valdivia, Michael J Ackerman, David J Tester, et al.
Mayo Clinic Proceedings|April 2, 2013
Institution-wide QT alert system identifies patients with a high risk of mortalityKristina H Haugaa, J Martijn Bos, Robert F Tarrell, et al.
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