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A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease

8 Sept 2023

Abstract excerpt

Background Chromosomal microarray analysis (CMA) provides an opportunity to understand genetic causes of congenital heart disease (CHD). The methods for describing cardiac phenotypes in patients with CMA abnormalities have been inconsistent, which may complicate clinical interpretation of abnormal testing results and hinder a more complete understanding of genotype–phenotype relationships. Methods and Results...

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PMID: 37681527
DOI: 10.1161/jaha.123.029340

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