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Integration of global SNP-based mapping and expression arrays reveals key regions, mechanisms, and genes important in the pathogenesis of multiple myeloma.

Blood - 1 Sept 2006

Walker Brian A, Leone Paola E, Jenner Matthew W, Li Cheng, Gonzalez David, Johnson David C, Ross Fiona M, Davies Faith E, Morgan Gareth J

Abstract excerpt

Multiple myeloma is characterized by genomic alterations frequently involving gains and losses of chromosomes. Single nucleotide polymorphism (SNP)-based mapping arrays allow the identification of copy number changes at the sub-megabase level and the identification of loss of heterozygosity (LOH) due to monosomy and uniparental disomy (UPD). We have found that SNP-based mapping array data and fluorescence in situ...

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Identifiers

PMID: 16705090
DOI: 10.1182/blood-2006-02-005496

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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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