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

Prevalence of chromosomal disorders in cases with congenital heart defect: registry‐based study from Denmark between 2008 and 2018

13 Sept 2022

Abstract excerpt

OBJECTIVE: To estimate the prevalence of chromosomal conditions in all fetuses and children with major congenital heart defect (CHD) in Denmark between 2008 and 2018. METHODS: This was a national registry-based study including all singleton pregnancies with a prenatally or postnatally diagnosed major CHD usually requiring surgery within the first year after birth and a due date between July 2008 and December 2018...

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 Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 36099538
DOI: 10.1002/uog.26075

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

Prevalence of chromosomal disorders in cases with congenital heart defect: registry‐based study from Denmark between 2008 and 2018PMID 36099538Read ↗

Clinical features and genetic analysis of 471 cases of fetal congenital heart disease: A systematic reviewSemantic proximity Read ↗

Clinical features and genetic analysis of 471 cases of fetal congenital heart disease.Semantic proximity Read ↗

Clinical Application of Chromosomal Microarray Analysis in Fetuses with Congenital Heart DiseaseSemantic proximity Read ↗

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

Chromosomal analysis and short-term outcome of prenatally diagnosed complex congenital heart diseaseSemantic proximity Read ↗

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

Other genomic disorders and congenital heart diseaseSemantic proximity Read ↗

The prevalence of genetic diagnoses in fetuses with severe congenital heart defectsSemantic proximity Read ↗

Congenital heart defects—chromosomal anomalies, syndromes and extracardiac malformationsSemantic proximity Read ↗

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

Personalized Genetic Diagnosis of Congenital Heart Defects in NewbornsSemantic proximity Read ↗

Diagnostic value of CMA in different phenotypes of fetal congenital heart defectsSemantic proximity Read ↗

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