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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...

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Literature Corpus work
ccd30c31-7d39-5da3-8438-2335adf80cb8
DOI
10.21203/rs.3.rs-3976548/v1
Open publication

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Rapid Genome Sequencing Shows Diagnostic Utility In Infants With Congenital Heart DefectsDOI 10.21203/rs.3.rs-3976548/v1
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