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Article

Identification of unbalanced genome copy number abnormalities in patients with multiple myeloma by single-nucleotide polymorphism genotyping microarray analysis.

International journal of hematology - 1 Oct 2012

Kamada Yuhei, Sakata-Yanagimoto Mamiko, Sanada Masashi, Sato-Otsubo Aiko, Enami Terukazu, Suzukawa Kazumi, Kurita Naoki, Nishikii Hidekazu, Yokoyama Yasuhisa, Okoshi Yasushi, Hasegawa Yuichi, Ogawa Seishi, Chiba Shigeru

Abstract excerpt

Single-nucleotide polymorphism genotyping microarray (SNP array) analysis provides detailed information on chromosomal copy number aberrations. To obtain detailed information on genomic abnormalities related to pathogenesis or prognosis of multiple myeloma (MM), we performed 250K SNP array analysis in 39 MM patients and 11 cell lines. We identified an accumulation of deletions and uniparental disomies at 22q12.1....

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 22972171
DOI: 10.1007/s12185-012-1171-1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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