Article
Rapid Genome Sequencing Shows Diagnostic Utility In Infants With Congenital Heart Defects
2024-03-20
Abstract excerpt
<title>Abstract</title> <p>Congenital heart disease (CHD) is the most common birth defect and a leading cause of infant mortality. CHD often has a genetic etiology and recent studies demonstrate utility in genetic testing. In clinical practice, decisions around genetic testing choices continue to evolve, and the incorporation of rapid genome sequencing (rGS) in CHD has not been well studied. Though smaller studie...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- ccd30c31-7d39-5da3-8438-2335adf80cb8
- DOI
- 10.21203/rs.3.rs-3976548/v1
