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

Analysis of Chromosomal Copy Number in First-Trimester Pregnancy Loss Using Next-Generation Sequencing

20 Oct 2020

Abstract excerpt

Embryonic chromosomal abnormality is one of the significant causative factors of early pregnancy loss. Our goal was to evaluate the clinical utility of next-generation sequencing (NGS) technology in identifying chromosomal anomalies associated with first-trimester pregnancy loss. In addition, we attempted to provide fertility guidance to couples anticipating a successful pregnancy. A total of 1,010 miscarriage...

Read the complete abstract on PubMed

Topics

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

Share to Congenital Anomalies and Fetal Surgery
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: 33193619
DOI: 10.3389/fgene.2020.545856

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of Chromosomal Copy Number in First-Trimester Pregnancy Loss Using Next-Generation SequencingPMID 33193619Read ↗

Chromosomal copy number variations in products of conception from spontaneous abortion by next-generation sequencing technologySemantic proximity Read ↗

Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencingSemantic proximity Read ↗

Experience of Copy number variation sequencing applied in production of conception from first- and second- trimester miscarriageSemantic proximity Read ↗

Chromosomal copy-number variation analysis of villous tissues using molecular karyotyping in early missed abortionsSemantic proximity Read ↗

Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy lossSemantic proximity Read ↗

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

Chromosomal Copy Number Variation Analysis in Pregnancy Products from Recurrent and Sporadic Miscarriage Using Next-Generation SequencingSemantic proximity Read ↗

A Novel System for the Detection of Spontaneous Abortion-Causing Aneuploidy and Its Erroneous Chromosome Origins through the Combination of Low-Pass Copy Number Variation Sequencing and NGS-Based STR TestsSemantic proximity Read ↗

Genetic analysis of chorionic villus tissues in early missed abortionsSemantic proximity Read ↗

Prevalence of chromosomal abnormalities identified by copy number variation sequencing in high-risk pregnancies, spontaneous abortions, and suspected genetic disordersSemantic proximity Read ↗

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

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

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