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Investigation of copy number variation in children with conotruncal heart defects

1 Jan 2014

Abstract excerpt

BACKGROUND: Congenital heart defects (CHD) are the most prevalent group of structural abnormalities at birth and one of the main causes of infant morbidity and mortality. Studies have shown a contribution of the copy number variation in the genesis of cardiac malformations. OBJECTIVES: Investigate gene copy number variation (CNV) in children with conotruncal heart defect. METHODS: Multiplex ligation-dependent...

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PMID: 25387403
DOI: 10.5935/abc.20140169

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