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Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2008
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and managementAngela E Lin, Craig T Basson, Elizabeth Goldmuntz, 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.
Human Mutation|March 13, 2018
Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errorsKathryn B Manheimer, Nihir Patel, Felix Richter, et al.
Circulation Research|February 16, 2013
The Congenital Heart Disease Genetic Network Study: rationale, design, and early results, Bruce Gelb, Martina Brueckner, et al.
Human Genetics|February 9, 2018
Robust identification of mosaic variants in congenital heart diseaseKathryn B Manheimer, Felix Richter, Lisa J Edelmann, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|February 13, 2025
Cardiovascular magnetic resonance imaging traits associated with adverse right ventricular remodeling in repaired tetralogy of Fallot: A Single Center Outcomes Using cardiovascular magnetic resonance in Tetralogy of Fallot studyElizabeth W Thompson, Ningiun J Dong, Jin-Seo Kim, et al.
Plos One|January 20, 2018
The Congenital Heart Disease Genetic Network Study: Cohort descriptionThanh T Hoang, Elizabeth Goldmuntz, Amy E Roberts, et al.
Plos Genetics|February 27, 2016
DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary DyskinesiaYou Li, Hisato Yagi, Ezenwa Obi Onuoha, et al.
Nature Communications|September 28, 2016
Loss of RNA expression and allele-specific expression associated with congenital heart diseaseDavid M McKean, Jason Homsy, Hiroko Wakimoto, et al.
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