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Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 28, 2006
What makes the heart fail? New insights from defective genesTimothy M OlsonPflugers Archiv : European Journal of Physiology|December 25, 2009
Human K(ATP) channelopathies: diseases of metabolic homeostasisTimothy M Olson, Andre TerzicJournal of Cardiovascular Development and Disease|April 21, 2022
Whole Genome Sequencing in Hypoplastic Left Heart SyndromeJeanne L Theis, Timothy M OlsonJournal of Cardiovascular Electrophysiology|February 13, 2008
X-linked nonsyndromic sinus node dysfunction and atrial fibrillation caused by emerin mutationMargaret L Karst, Kathleen J Herron, Timothy M OlsonAmerican Journal of Medical Genetics. Part A|February 24, 2015
Exome sequencing establishes diagnosis of Alström syndrome in an infant presenting with non-syndromic dilated cardiomyopathyPamela A Long, Jared M Evans, Timothy M OlsonJournal of Cardiovascular Development and Disease|September 29, 2017
Modeling GATAD1-Associated Dilated Cardiomyopathy in Adult ZebrafishJingchun Yang, Sahrish Shah, Timothy M Olson, et al.The American Journal of Cardiology|April 13, 2011
Uncovering an intermediate phenotype associated with rs2200733 at 4q25 in lone atrial fibrillationAdele H Goodloe, Kathleen J Herron, Timothy M OlsonCardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|January 18, 2006
Congenital heart defects in siblings with partial aneuploidy of chromosome 2pCarolyn A Morris, Thomas M Sutton, Timothy M OlsonJournal of Cardiovascular Development and Disease|January 26, 2018
Diagnostic Yield of Whole Exome Sequencing in Pediatric Dilated CardiomyopathyPamela A Long, Jared M Evans, Timothy M OlsonThe American Journal of Cardiology|May 12, 2009
Comprehensive mutation scanning of LMNA in 268 patients with lone atrial fibrillationKatharine M Brauch, Lin Y Chen, Timothy M OlsonPageof 8