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Article

High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs.

American journal of human genetics - 1 Nov 2005

Slater Howard R, Bailey Dione K, Ren Hua, Cao Manqiu, Bell Katrina, Nasioulas Steven, Henke Robert, Choo K H Andy, Kennedy Giulia C

Abstract excerpt

Mutation of the human genome ranges from single base-pair changes to whole-chromosome aneuploidy. Karyotyping, fluorescence in situ hybridization, and comparative genome hybridization are currently used to detect chromosome abnormalities of clinical significance. These methods, although powerful, suffer from limitations in speed, ease of use, and resolution, and they do not detect copy-neutral chromosomal...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 16252233
DOI: 10.1086/497343
PMCID: PMC1271402

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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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