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Article

Cardiovascular Anomalies Associated With Chromosome 22q11.2 Deletion Syndrome

22 May 2010

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 20494672
DOI: 10.1016/j.amjcard.2010.01.333

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Cardiovascular Anomalies Associated With Chromosome 22q11.2 Deletion SyndromePMID 20494672Read ↗

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiersSemantic proximity Read ↗

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Transposition of the great arteries associated with deletion of chromosome 22q11Semantic proximity Read ↗

Extracardiac features predicting 22q11.2 Deletion Syndrome in adult congenital heart diseaseSemantic proximity Read ↗

The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population‐based studySemantic proximity Read ↗

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

Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromesSemantic proximity Read ↗

Prenatal diagnosis of aneuploidy and deletion 22q11.2 in fetuses with ultrasound detection of cardiac defectsSemantic proximity Read ↗

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndromeSemantic proximity Read ↗

Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome.Semantic proximity Read ↗

[Extra-cardiac phenotype associated with microdeletion 22q11].Semantic proximity Read ↗

The 22q11.2 deletion: from diversity to a single gene theory.Semantic proximity Read ↗

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