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Article

Prenatal diagnosis of aneuploidy and deletion 22q11.2 in fetuses with ultrasound detection of cardiac defects

1 Dec 2004

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Share to Congenital heart defects research
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15592293
DOI: 10.1016/j.ajog.2004.05.022

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Prenatal diagnosis of aneuploidy and deletion 22q11.2 in fetuses with ultrasound detection of cardiac defectsPMID 15592293Read ↗

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

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Rare and Complex Cardiac Anomalies Associated with 22q11.2 Deletion: An Ultrasonographic Visual Trip from Diagnosis until DeliverySemantic proximity Read ↗

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

Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome.Semantic proximity Read ↗

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

A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomesSemantic proximity Read ↗

Prenatal Screening and Diagnostic Considerations for 22q11.2 MicrodeletionsSemantic proximity Read ↗

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

Congenital heart disease and aneuploidySemantic proximity Read ↗

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

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