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Article

Analysis of Genomic Copy Number Variation in Miscarriages During Early and Middle Pregnancy

17 Sept 2021

Abstract excerpt

The purpose of this study was to explore the copy number variations (CNVs) associated with miscarriage during early and middle pregnancy and provide useful genetic guidance for pregnancy and prenatal diagnosis. A total of 505 fetal specimens were collected and CNV sequencing (CNV-seq) analysis was performed to determine the types and clinical significance of CNVs, and relevant medical records were collected. The...

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Share to Congenital Anomalies and Fetal Surgery
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

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Identifiers

PMID: 34603391
DOI: 10.3389/fgene.2021.732419

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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