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Article

Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths.

Prenatal diagnosis - 1 Oct 2011

Harris R Alan, Ferrari Francesca, Ben-Shachar Shay, Wang Xiaoling, Saade George, Van Den Veyver Ignatia, Facchinetti Fabio, Aagaard-Tillery Kjersti

Abstract excerpt

OBJECTIVE: Accumulating evidence suggests that genomic structural variations, particularly copy number variations (CNV), are a common occurrence in humans that may bear phenotypic consequences for living individuals possessing the variant. While precise estimates vary, large-scale karyotypic abnormalities are present in 6-12% of stillbirths (SB). However, due to inherent limitations of conventional cytogenetics,...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 21732394
DOI: 10.1002/pd.2817
PMCID: PMC3183137

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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