Chromosomal and genetic abnormalities in myeloma

Author:

Joy Ho P.

Publisher

Wiley

Subject

Hematology

Reference70 articles.

1. Cytogenetic, interphase, and multicolor fluorescence in situ hybridization analyses in primary plasma cell leukemia: a study of 40 patients at diagnosis, on behalf of the Intergroupe Francophone du Myelome and the Groupe Francais de Cytogenetique Hematologique;Avet-Loiseau;Blood,2001a

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

3. 14q32 translocations and monosomy 13 observed in monoclonal gammopathy of undetermined significance delineate a multistep process for the oncogenesis of multiple myeloma;Avet-Loiseau;Cancer Research,1999a

4. Rearrangements of the c-myc oncogene are present in 15% of primary human multiple myeloma tumors;Avet-Loiseau;Blood,2001b

5. 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

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