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2. Timing of acquisition of deletion 13 in plasma cell dyscrasias is dependent on genetic context. Chiecchio L, Dagrada GP, Ibrahim AH, Dachs Cabanas E, Protheroe RK, Stockley DM, Orchard KH, Cross NC, Harrison CJ, Ross FM, UK Myeloma Forum. Haematologica; 2009 Dec; 94(12):1708-13. PubMed ID: 19996118 [Abstract] [Full Text] [Related]
3. Molecular cytogenetic aberrations in patients with multiple myeloma studied by interphase fluorescence in situ hybridization. Chen L, Li J, Xu W, Qiu H, Zhu Y, Zhang Y, Duan L, Qian S, Lu H. Exp Oncol; 2007 Jun; 29(2):116-20. PubMed ID: 17704743 [Abstract] [Full Text] [Related]
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5. The Ig heavy chain gene is frequently involved in chromosomal translocations in multiple myeloma and plasma cell leukemia as detected by in situ hybridization. Nishida K, Tamura A, Nakazawa N, Ueda Y, Abe T, Matsuda F, Kashima K, Taniwaki M. Blood; 1997 Jul 15; 90(2):526-34. PubMed ID: 9226151 [Abstract] [Full Text] [Related]
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11. 14q32 translocations and monosomy 13 observed in monoclonal gammopathy of undetermined significance delineate a multistep process for the oncogenesis of multiple myeloma. Intergroupe Francophone du Myélome. Avet-Loiseau H, Facon T, Daviet A, Godon C, Rapp MJ, Harousseau JL, Grosbois B, Bataille R. Cancer Res; 1999 Sep 15; 59(18):4546-50. PubMed ID: 10493504 [Abstract] [Full Text] [Related]
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