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Pediatric Neurology|July 29, 2020
Cerebrovascular Malformations in a Pediatric Hereditary Hemorrhagic Telangiectasia CohortLauren A Beslow, Jake Breimann, Daniel J Licht, et al.
American Journal of Human Genetics|March 13, 2003
Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defectsSusan W Robinson, Cynthia D Morris, Elizabeth Goldmuntz, et al.
Journal of the American College of Cardiology|September 21, 2019
2-Year Outcomes After Complete or Staged Procedure for Tetralogy of Fallot in NeonatesJill J Savla, Jennifer A Faerber, Yuan-Shung V Huang, et al.
International Journal of Cardiology|April 29, 2022
Comparison of serum biomarkers of myocardial fibrosis with cardiac magnetic resonance in patients operated for tetralogy of FallotMichael P DiLorenzo, Grace DeCost, Anh Duc Mai, et al.
American Journal of Medical Genetics. Part A|September 9, 2016
Utility of genetic evaluation in infants with congenital heart defects admitted to the cardiac intensive care unitRebecca C Ahrens-Nicklas, Shama Khan, Jennifer Garbarini, et al.
Biodata Mining|February 13, 2022
Gene-Interaction-Sensitive enrichment analysis in congenital heart diseaseAlexa A Woodward, Deanne M Taylor, Elizabeth Goldmuntz, et al.
The American Journal of Cardiology|December 3, 2014
Trends in pulmonary valve replacement in children and adults with tetralogy of fallotMichael L O'Byrne, Andrew C Glatz, Laura Mercer-Rosa, et al.
Human Molecular Genetics|August 21, 2014
Genome-wide association study of maternal and inherited effects on left-sided cardiac malformationsLaura E Mitchell, A J Agopian, Angela Bhalla, et al.
Birth Defects Research|April 12, 2017
Rare copy number variants in patients with congenital conotruncal heart defectsHongbo M Xie, Petra Werner, Dwight Stambolian, et al.
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