Article

Evaluating the link between chromosomal abnormalities and diminished ovarian reserve, mode of conception, and history of prior miscarriages in cases of early missed abortion using CNV-seq

2024-07-26

Abstract excerpt

<title>Abstract</title> <p> <bold>Objective:</bold> This study was developed as a retrospective analysis of the rates of embryonic chromosomal abnormalities in cases of missed miscarriages during early pregnancy, with a focus on identifying associated factors as a means of clarifying the genetic basis for missed miscarriages and how this pregnancy outcome relates to a variety of clinical and demographic charact...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 93f3e4cf-9ccd-572e-b743-c70c510dd901
DOI: 10.21203/rs.3.rs-4641482/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Evaluating the link between chromosomal abnormalities and diminished ovarian reserve, mode of conception, and history of prior miscarriages in cases of early missed abortion using CNV-seqDOI 10.21203/rs.3.rs-4641482/v1Read

Genetic analysis of chorionic villus tissues in early missed abortionsSemantic 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

A clinical study of CNV-seq techniques in 103 cases of spontaneous abortionSemantic proximity Read

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

Chromosomal Analysis of 129 Miscarried Conceptuses: A Retrospective StudySemantic proximity Read

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

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

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