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Article

Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China.

Scientific reports - 4 May 2023

Cai Meiying, Lin Na, Guo Nan, Su Linjuan, Wu Xiaoqing, Xie Xiaorui, Li Ying, He Shuqiong, Fu Xianguo, Xu Liangpu, Huang Hailong

Abstract excerpt

Numerous studies have evaluated the use of single nucleotide polymorphism array (SNP-array) in prenatal diagnostics, but very few have evaluated its application under different risk conditions. Here, SNP-array was used for the retrospective analysis of 8386 pregnancies and the cases were categorized into seven groups. Pathogenic copy number variations (pCNVs) were found in 699 (8.3%, 699/8386) cases. Among the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 37142625
DOI: 10.1038/s41598-023-33668-0
PMCID: PMC10160013

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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