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

Right-sided aortic arch in the age of microarray.

Prenatal diagnosis - 1 May 2017

O'Mahony Edward F, Hutchinson Darren P, McGillivray George, Nisbet Debbie L, Palma-Dias Ricardo

Abstract excerpt

OBJECTIVE: For fetuses with a diagnosis of right aortic arch and normal cardiac anatomy, we aimed to establish the frequency of chromosomal anomaly diagnosed with single nucleotide polymorphism microarray analysis, particularly focusing on microduplications or microdeletions which would have gone undetected by conventional karyotyping and six-probe fish (13,18,21, X,Y, TUPLE). METHOD: Retrospective study of fetal...

Read the complete abstract on PubMed

Topics

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

Share to Aorta, Thoracic
Share to Chromosome Disorders
Share to Heart Defects, Congenital

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Karyotyping

Share to Microarray Analysis

Share to Pregnancy

Share to Prenatal Diagnosis

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 28207948
DOI: 10.1002/pd.5029

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

Right-sided aortic arch in the age of microarray.PMID 28207948Read ↗

Fetal right aortic arch: associated anomalies, genetic anomalies with chromosomal microarray analysis, and postnatal outcomeSemantic proximity Read ↗

Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype.Semantic proximity Read ↗

Chromosomal microarray analysis in fetuses with aberrant right subclavian arterySemantic proximity Read ↗

Fetal double aortic arch: prenatal sonographic and postnatal computed tomography angiography features, associated abnormalities and clinical outcomesSemantic proximity Read ↗

Chromosomal abnormalities and pregnancy outcomes in 350 pregnancies with prenatally diagnosed aberrant right subclavian artery: a phenotype-based retrospective cohort study.Semantic proximity Read ↗

A Prenatal Ultrasound Diagnosis of an A-Type Persistent Fifth Aortic Arch: A Case ReportSemantic proximity Read ↗

Isolated aberrant right subclavian artery: an underlying clue for genetic anomaliesSemantic proximity Read ↗

22q11 deletions in fetuses with malformations of the outflow tracts or interruption of the aortic arch: impact of additional ultrasound signsSemantic proximity Read ↗

Variation in prevalence of chromosome 22q11 deletion in subtypes of conotruncal defect in 254 children.Semantic proximity Read ↗

Fetal Aberrant Right Subclavian Artery: Associated Anomalies, Genetic Etiology, and Postnatal Outcomes in a Retrospective Cohort StudySemantic proximity Read ↗

Fetal Aberrant Right Subclavian Artery: Associated Anomalies, Genetic Etiology, and Postnatal Outcomes in a Retrospective Cohort StudySemantic proximity Read ↗

Aberrant right subclavian artery: embryology, prenatal diagnosis and clinical significanceSemantic proximity Read ↗

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