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• W2597263729 endingPage "940" @default.
• W2597263729 startingPage "923" @default.
• W2597263729 abstract "Congenital heart disease is the most common birth defect, and because of major advances in medical and surgical management, there are now more adults living with congenital heart disease (CHD) than children. Until recently, the cause of the majority of CHD was unknown. Advances in genomic technologies have discovered the genetic causes of a significant fraction of CHD, while at the same time pointing to remarkable complexity in CHD genetics. This review will focus on the evidence for genetic causes underlying CHD and discuss data supporting both monogenic and complex genetic mechanisms underlying CHD. The discoveries from CHD genetic studies draw attention to biological pathways that simultaneously open the door to a better understanding of cardiac development and affect clinical care of patients with CHD. Finally, we address clinical genetic evaluation of patients and families affected by CHD." @default.
• W2597263729 created "2017-03-23" @default.
• W2597263729 creator A5002562071 @default.
• W2597263729 creator A5085090650 @default.
• W2597263729 date "2017-03-17" @default.
• W2597263729 modified "2023-10-17" @default.
• W2597263729 title "Genetics and Genomics of Congenital Heart Disease" @default.
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