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Article

Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencing

17 Oct 2023

Abstract excerpt

Introduction: Embryonic chromosomal abnormalities represent a major causative factor in early pregnancy loss, highlighting the importance of understanding their role in spontaneous abortion. This study investigates the potential correlation between chromosomal abnormalities and spontaneous abortion using copy number variation sequencing (CNV-seq), a Next-Generation Sequencing (NGS) technology. Methods: We...

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Share to Assisted Reproductive Technology and Twin Pregnancy
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 37916154
DOI: 10.3389/fendo.2023.1218793

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

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