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

Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype.

Molecular diagnosis & therapy - 1 Oct 2020

Wu Xiaoqing, Li Ying, Su Linjuan, Xie Xiaorui, Cai Meiying, Lin Na, Huang Hailong, Lin Yuan, Xu Liangpu

Abstract excerpt

BACKGROUND: Aortic arch abnormalities (AAA) are abnormal embryologic developments of the aorta and its branches. Their outcomes often depend on their association with other congenital diseases and genetic testing results. OBJECTIVE: This study aimed to evaluate the yield of chromosomal microarray analysis (CMA) in fetuses with different patterns of AAA and normal karyotype. METHODS: Data from 158 pregnancies...

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 Aberrations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heart Defects, Congenital

Share to Karyotype

Share to Karyotyping

Share to Prenatal Diagnosis

Share to Ultrasonography, Prenatal

Source

Open in PubMed Open full text

Identifiers

PMID: 32651932
DOI: 10.1007/s40291-020-00474-7
PMCID: PMC7497298

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype.PMID 32651932Read ↗

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

Right-sided aortic arch in the age of microarray.Semantic proximity Read ↗

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

Prenatal chromosomal microarray analysis in a large Chinese cohort of fetuses with congenital heart defects: a single center studySemantic 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 ↗

Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study.Semantic proximity Read ↗

Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound.Semantic proximity Read ↗

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

What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?Semantic proximity Read ↗

Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in FranceSemantic proximity Read ↗

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

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