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

Systematic analysis of copy‐number variations associated with early pregnancy loss

31 Jul 2019

Abstract excerpt

OBJECTIVES: Embryonic numerical and structural chromosomal abnormalities are the most common cause of early pregnancy loss. However, the role of submicroscopic copy-number variations (CNVs) in early pregnancy loss is unclear, and little is known about the critical regions and candidate genes for miscarriage, because of the large size of structural chromosomal abnormalities. The aim of this study was to identify...

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: 31364215
DOI: 10.1002/uog.20412

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Systematic analysis of copy‐number variations associated with early pregnancy lossPMID 31364215Read ↗

Genomic characteristics of miscarriage copy number variantsSemantic proximity Read ↗

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

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

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

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

Clinical utilization of chromosomal microarray analysis for the genetic analysis in subgroups of pregnancy lossSemantic proximity Read ↗

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

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

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

Analysis of potential copy-number variations and genes associated with first-trimester missed abortionSemantic proximity Read ↗

Analysis of copy number variations and candidate genes in recurrent pregnancy loss.Semantic proximity Read ↗

The genomic basis of sporadic and recurrent pregnancy loss: a comprehensive in-depth analysis of 24,900 miscarriagesSemantic proximity Read ↗

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