The recurrent translocation t(14;20)(q32;q12) in multiple myeloma results in aberrant expression of MAFB : a molecular and genetic analysis of the chromosomal breakpoint
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2004.05050.x/fullpdf
Reference24 articles.
1. Oncogenesis of multiple myeloma: 14q32 and 13q chromosomal abnormalities are not randomly distributed, but correlate with natural history, immunological features, and clinical presentation;Avet-Loiseau;Blood,2002
2. A lymphocyte-specific cellular enhancer is located downstream of the joining region in immunoglobulin heavy chain genes;Banerji;Cell,1983
3. Chromosome translocations in multiple myeloma;Bergsagel;Oncogene,2001
4. Translocation of the IgH locus is nearly ubiquitous in multiple myeloma as detected by immuno-FISH;Boersma-Vreugdenhil;Blood,2003
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