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Article

Analysis of potential copy-number variations and genes associated with first-trimester missed abortion

1 Aug 2023

Abstract excerpt

Background Copy number variation sequencing (CNV-seq) was proven to be a highly effective tool in studying of chromosomal copy number variations (CNVs) in prenatal diagnosis and post-natal cases with developmental abnormalities. However, the overall characteristics of missed abortion (MA) CNVs were largely unexplored. Methods We retrospectively analyzed the results of CNV-seq in first-trimester MA. The samples...

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Share to Fetal and Pediatric Neurological Disorders
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PMID: 37593615
DOI: 10.1016/j.heliyon.2023.e18868

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