Haematologica
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Haematologica, Vol 82, Issue 3, 336-337
Copyright © 1997 by Ferrata Storti Foundation


Case Reports

Duplication of the der(13)t(12;13)(p13;q14) in chronic myelomonocytic leukemia

G Fugazza, R Cerri, R Bruzzone, F Patrone, and M Sessarego

Department of Internal Medicine (DIMI), University of Genoa, Italy.

A case of chronic myelomonocytic leukemia with a reciprocal translocation (12;13)(p13;q14) and other numerical and structural abnormalities is described. Most of the metaphases examined showed duplication of the der(13)t(12;13), leading to trisomy of the translocated segment of chromosome 12. Using fluorescence in situ hybridization we observed that the breakpoint on chromosome 13 is centromeric to the retinoblastoma gene. Since other cases with apparently similar t(12;13) have recently been reported, we conclude that this structural rearrangement may be a rare but non random event in hematologic disorders.


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A. Chase, A. Reiter, L. Burci, G. Cazzaniga, A. Biondi, J. Pickard, I. A.G. Roberts, J. M. Goldman, and N. C.P. Cross
Fusion of ETV6 to the Caudal-Related Homeobox Gene CDX2 in Acute Myeloid Leukemia With the t(12;13)(p13;q12)
Blood, February 1, 1999; 93(3): 1025 - 1031.
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