Cytogenetics of multiple myeloma: interpretation of fluorescence in situ hybridization results

Author:

Harrison Christine J.,Mazzullo Helen,Cheung Kan L.,Gerrard Gareth,Jalali G. Reza,Mehta Atul,Osier David G.,Orchard Kim H.

Publisher

Wiley

Subject

Hematology

Reference48 articles.

1. Molecular cytogenetic abnormalities in multiple myeloma and plasma cell leukemia measured using comparative genomic hybridization;Avet-Loiseau;Genes, Chromosomes and Cancer,1997

2. High incidence of translocations t(11;14)(q13;q32) and t(4;14)(p16;q32) in patients with plasma cell malignancies;Avet-Loiseau;Cancer Research,1998

3. Chromosome 13 abnormalities in multiple myeloma are mostly monosomy 13;Avet-Loiseau;British Journal of Haematology,2000a

4. 14q32 chromosomal translocations: a hallmark of plasma cell dyscrasias?;Avet-Loiseau;Hematology Journal,2000b

5. 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

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