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Article

Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects

14 Mar 2018

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Share to Congenital heart defects research
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Share to Genomic variations and chromosomal abnormalities

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 29541814
DOI: 10.1007/s00246-018-1842-7

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Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart DefectsPMID 29541814Read ↗

The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart diseaseSemantic proximity Read ↗

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Submicroscopic Chromosomal Copy Number Variations Identified in Children With Hypoplastic Left Heart SyndromeSemantic proximity Read ↗

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Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosisSemantic proximity Read ↗

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