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June 10, 2024

[Feasibility of non-invasive prenatal testing for the detection of fetal chromosomal copy number variants].

Xue Ying Longwei Qiao Quanze He Chunhua Zhang Xiaojuan Wu Guodong Zhao Ting Wang

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Abstract

To explore the feasibility of non-invasive prenatal testing (NIPT) for detecting fetal chromosomal copy number variants (CNV).

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Cite This Study

Ying et al. (2024) studied this question.

synapsesocial.com/papers/68e65761b6db6435875e5d45 https://doi.org/10.3760/cma.j.cn511374-20220504-00304

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Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Efficiency of Non-Invasive Prenatal Testing in Detecting Fetal Copy Number Variation: A Retrospective Cohort Study2024 · 3 citations
2Copy Number Variant Detection by NIPT: Biological Constraints and the Limits of Prenatal Genomic InferenceReview · 2026
3Clinical Performance Evaluation of Size‐Selective Placental Cell‐Free DNA Enrichment for Non‐Invasive Prenatal Testing of Fetal Copy Number VariantsRetrospective Study · 2026
4Accuracy of expanded noninvasive prenatal testing for maternal copy number variations: A comparative study with CNV-seq of maternal lymphocyte DNA2024 · 4 citations
5Application of CNV-seq combined with chromosome karyotyping in prenatal diagnosis of pregnant women with high-risk NIPT resultsOriginal Research · 2026