Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

16 Sept 2010

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Congenital heart defects research
Share to Congenital Heart Disease Studies
Share to Coronary Artery Anomalies

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 20848279
DOI: 10.1007/s00246-010-9763-0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Investigating 22q11.2 Deletion and Other Chromosomal Aberrations in Fetuses With Heart Defects Detected by Prenatal EchocardiographyPMID 20848279Read ↗

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

Extracardiac features predicting 22q11.2 Deletion Syndrome in adult congenital heart diseaseSemantic 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 diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiersSemantic proximity Read ↗

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

Other genomic disorders and congenital heart diseaseSemantic proximity Read ↗

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

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

Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound.Semantic proximity Read ↗

Prevalence of associated extracardiac anomalies in prenatally diagnosed congenital heart diseasesSemantic proximity Read ↗

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

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

⌁Select a neighboring publication to make it the new centre.