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 Abnormalities Detected by Chromosomal Microarray Analysis and Karyotype in Fetuses with Ultrasound Abnormalities

1 Oct 2024

Abstract excerpt

Objective: Chromosomal microarray analysis (CMA) is a first-line test to assess the genetic etiology of fetal ultrasound abnormalities. The aim of this study was to evaluate the effectiveness of CMA in detecting chromosomal abnormalities in fetuses with ultrasound abnormalities, including structural abnormalities and non-structural abnormalities. Methods: A retrospective study was conducted on 368 fetuses with...

Read the complete abstract on PubMed

Topics

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

Share to Fetal and Pediatric Neurological Disorders
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: 39429961
DOI: 10.2147/ijgm.s483290

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Chromosomal Abnormalities Detected by Chromosomal Microarray Analysis and Karyotype in Fetuses with Ultrasound AbnormalitiesPMID 39429961Read ↗

A retrospective study for diagnostic value of chromosomal microarray analysis in fetuses with high-risk prenatal indicationsSemantic proximity Read ↗

Chromosomal Microarray Analysis and Karyotype Analysis for Prenatal Diagnosis of Fetuses With Abnormal Ultrasound Soft MarkersSemantic proximity Read ↗

Prenatal Diagnosis Using Chromosomal Microarray Analysis in High-Risk PregnanciesSemantic proximity Read ↗

Clinical application of chromosome microarray analysis and karyotyping in prenatal diagnosis in Northwest ChinaSemantic proximity Read ↗

Chromosome microarray analysis combined with karyotype analysis is a powerful tool for the detection in pregnant women with high-risk indicatorsSemantic proximity Read ↗

Clinical Application of Chromosomal Microarray Analysis in High-Risk PregnanciesSemantic proximity Read ↗

Comparison of chromosomal microarray and karyotyping in prenatal diagnosis using 491 amniotic fluid samplesSemantic proximity Read ↗

The Diagnostic Utility of Prenatal Microarray in High-Risk Pregnancies: A Single-Center Experience to Enhance Reproductive Care and Risk StratificationSemantic proximity Read ↗

Application of chromosome microarray analysis in prenatal diagnosisSemantic proximity Read ↗

Potentials and challenges of chromosomal microarray analysis in prenatal diagnosisSemantic proximity Read ↗

Application of chromosomal microarray analysis in congenital heart diseaseSemantic proximity Read ↗

Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive casesSemantic proximity Read ↗

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