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

Prenatal diagnosis by chromosomal microarray analysis.

Fertility and sterility - 1 Feb 2018

Levy Brynn, Wapner Ronald

Abstract excerpt

Chromosomal microarray analysis (CMA) is performed either by array comparative genomic hybridization or by using a single nucleotide polymorphism array. In the prenatal setting, CMA is on par with traditional karyotyping for detection of major chromosomal imbalances such as aneuploidy and unbalanced rearrangements. CMA offers additional diagnostic benefits by revealing sub-microscopic imbalances or copy number...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Disorders
Share to Chromosome Duplication
Share to Chromosomes, Human

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Comparative Genomic Hybridization

Share to Genetic Counseling

Share to Karyotyping

Share to Prenatal Diagnosis

Share to Ultrasonography, Prenatal

Source

Open in PubMed Open full text

Identifiers

PMID: 29447663
DOI: 10.1016/j.fertnstert.2018.01.005
PMCID: PMC5856154

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prenatal diagnosis by chromosomal microarray analysis.PMID 29447663Read ↗

Chromosomal Microarray Analysis and Prenatal DiagnosisSemantic proximity Read ↗

Chromosomal Microarrays for the Prenatal Detection of Microdeletions and Microduplications.Semantic proximity Read ↗

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

Microarray comparative genomic hybridization in prenatal diagnosis: a reviewSemantic proximity Read ↗

Microarray-based prenatal diagnosis for the identification of fetal chromosome abnormalities.Semantic proximity Read ↗

Chromosomal Microarray versus Karyotyping for Prenatal DiagnosisSemantic proximity Read ↗

Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnanciesSemantic proximity Read ↗

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital AnomaliesSemantic proximity Read ↗

Experience with microarray‐based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnanciesSemantic proximity Read ↗

Chromosomal Microarray Versus Karyotyping for Prenatal DiagnosisSemantic proximity Read ↗

Evolving applications of microarray analysis in prenatal diagnosis.Semantic proximity Read ↗

Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital AnomaliesSemantic proximity Read ↗

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