Common features of myeloproliferative disorders with t(8;9)(p12;q33) and CEP110–FGFR1 fusion: Report of a new case and review of the literature

Author:

Mozziconacci Marie-Joëlle,Carbuccia Nadine,Prebet Thomas,Charbonnier Aude,Murati Anne,Vey Norbert,Chaffanet Max,Birnbaum Daniel

Publisher

Elsevier BV

Subject

Cancer Research,Oncology,Hematology

Reference14 articles.

1. FGFR is fused to the centrosome-associated protein CEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33);Guasch;Blood,2000

2. A further case of acute myelomonocytic leukemia with inv(8) chromosomal rearrangement and MOZ-NCOA2 gene fusion;Murati;Int J Mol Med,2003

3. Rearrangements involving chromosome 12q arm in myeloproliferative disorders: possible role of HMGA2 and SOCS2 genes;Etienne;Cancer Genet Cytogenet,2007

4. Novel reciprocal translocation between chromosomes 8 and 9 found in a patient with myeloproliferative disorder;Friedhoff;Cancer Genet Cytogenet,1983

5. Philadelphia chromosome negative chronic myelogenous leukemia in a child with t(8;9)(p11 or 12;q34);Lewis;Am J Pediatr hematol Oncol,1983

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