A novel t(3;17)(p25;q21) variant translocation of acute promyelocytic leukemia with rearrangement of the RARA locus

Author:

Redner R L,Contis L C,Craig F,Evans C,Sherer M E,Shekhter-Levin S

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Cancer Research,Hematology

Reference8 articles.

1. Melnick A, Licht JD . Deconstructing a disease: RARalpha, its fusion partners, and their roles in the pathogenesis of acute promyelocytic leukemia. Blood 1999; 93: 3167–3215.

2. Grimwade D, Biondi A, Mozziconacci MJ, Hagemeijer A, Berger R, Neat M et al. Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17): results of the European Working Party* Groupe Francais de Cytogenetique Hematologique, Groupe de Francais d’Hematologie Cellulaire, UK Cancer Cytogenetics Group and BIOMED 1 European Community-Concerted Action ‘Molecular Cytogenetic Diagnosis in Haematological Malignancies’. Blood 2000; 96: 1297–1308.

3. Redner RL . Variations on a theme: the alternate translocations in APL. Leukemia 2002; 16: 1927–1932.

4. Miyakis S, Liloglou T, Kearney S, Xinarianos G, Spandidos DA, Field JK . Absence of mutations in the VHL gene but frequent loss of heterozygosity at 3p25–26 in non-small cell lung carcinomas. Lung Cancer 2003; 39: 273–277.

5. Yang Q, Yoshimura G, Mori I, Sakurai T, Kakudo K . Chromosome 3p and breast cancer. J Hum Genet 2002; 47: 453–459.

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