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Article

Identification of chromosomal abnormalities in miscarriages using single-nucleotide polymorphism arrays.

Archives of gynecology and obstetrics - 10 Jun 2026

Zhao Wantong, Wang Haiwei, Liang Bin, Huang Hailong, Lin Na, Xu Liangpu

Abstract excerpt

PURPOSE: Chromosome abnormalities are a known cause of miscarriage. A detailed chromosomal study in miscarriages is delineated using high-throughput technologies. METHODS: 564 miscarriages were collected, and the chromosomal abnormalities, including triploidy, trisomy, monosomy, uniparental disomy, and chromosomal deletions/duplications in miscarriages, were detected by high-throughput single-nucleotide...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 42271033
DOI: 10.1007/s00404-026-08337-y
PMCID: PMC13478020

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

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