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Article

Extracardiac features predicting 22q11.2 Deletion Syndrome in adult congenital heart disease

14 Jan 2008

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 18191243
DOI: 10.1016/j.ijcard.2007.08.141

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Extracardiac features predicting 22q11.2 Deletion Syndrome in adult congenital heart diseasePMID 18191243Read ↗

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Associated genetic syndromes and extracardiac malformations strongly influence outcomes of fetuses with congenital heart diseasesSemantic proximity Read ↗

Investigating 22q11.2 Deletion and Other Chromosomal Aberrations in Fetuses With Heart Defects Detected by Prenatal EchocardiographySemantic proximity Read ↗

Genetic syndromes associated with congenital heart disease.Semantic proximity Read ↗

Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: A prospective studySemantic proximity Read ↗

Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome.Semantic proximity Read ↗

Congenital heart defects and 22q11 deletions: which genes count?Semantic proximity Read ↗

Cardiovascular Anomalies Associated With Chromosome 22q11.2 Deletion SyndromeSemantic proximity Read ↗

Conotruncal Heart Defects: A Narrative Review of Molecular Genetics, Genomics Research and Innovation.Semantic proximity Read ↗

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndromeSemantic proximity Read ↗

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