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

Clinical utilization of chromosomal microarray analysis for the genetic analysis in subgroups of pregnancy loss

23 Nov 2020

Abstract excerpt

OBJECTIVE: The underlying etiologies of pregnancy loss are heterogeneous and in many cases unexplained. This study was to explore the genetic causes of early and late pregnancy loss using chromosomal microarray analysis (CMA). METHODS: A cohort of 222 specimens of conceptions underwent genetic analysis using Affymetrix CytoScan 750 K arrays, which includes both SNP markers and copy number markers. RESULTS: Of the...

Read the complete abstract on PubMed

Topics

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

Share to Gestational Trophoblastic Disease Studies
Share to Prenatal Screening and Diagnostics
Share to Reproductive System and Pregnancy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 33228446
DOI: 10.1080/14767058.2020.1849126

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical utilization of chromosomal microarray analysis for the genetic analysis in subgroups of pregnancy lossPMID 33228446Read ↗

Chromosomal Aneuploidy Associated With Clinical Characteristics of Pregnancy LossSemantic proximity Read ↗

Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.Semantic proximity Read ↗

Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral centerSemantic proximity Read ↗

Characterization of Copy-Number Variations and Possible Candidate Genes in Recurrent Pregnancy Losses.Semantic proximity Read ↗

Analysis of Chromosomal Copy Number in First-Trimester Pregnancy Loss Using Next-Generation SequencingSemantic proximity Read ↗

Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.Semantic proximity Read ↗

Enhanced genetic diagnosis in early pregnancy loss: an integrated approach using CNV-Seq and STR genotyping.Semantic proximity Read ↗

Recurrent pregnancy loss evaluation combined with 24-chromosome microarray of miscarriage tissue provides a probable or definite cause of pregnancy loss in over 90% of patientsSemantic proximity Read ↗

Analysis of Genomic Copy Number Variation in Miscarriages During Early and Middle PregnancySemantic proximity Read ↗

Differentiation of genetic abnormalities in early pregnancy lossSemantic proximity Read ↗

Chromosomal copy number variations in miscarriages and the geneic counseling of recurrent pregnancy lossSemantic proximity Read ↗

Cytogenetic signatures of recurrent pregnancy lossesSemantic proximity Read ↗

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