t(4;14)(p16.3;q32) is strongly associated with a shorter survival in myeloma patients

Author:

Winkler Jerry M.,Greipp Philip R.,Fonseca Rafael

Publisher

Wiley

Subject

Hematology

Reference5 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. Promiscuous translocations into immunoglobulin heavy chain switch regions in multiple myeloma;Bergsagel;Proceedings of the National Academy of Sciences of the United States of America,1996

3. A molecular classification of multiple myeloma (MM), based on cytogenetic abnormalities detected by interphase FISH, is powerful in identifying discrete groups of patients with dissimilar prognosis;Fonseca;Blood,2001

4. Translocation t(4;14) (p16.3;q32) is a recurrent genetic lesion in primary amyloidosis;Perfetti;Leukemia,2001

5. FGFR3 dysregulation in multiple myeloma: frequency and prognostic relevance;Rasmussen;British Journal of Haematology,2002

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