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Updated: Jul 18, 2026

FISH for Pre-implantation Genetic Diagnosis
Published on: February 23, 2011
Translocation (10;17)(p15;q21) is a recurrent anomaly in acute myeloblastic leukemia
Adrian Tempescul1, Gaëlle Guillerm, Nathalie Douet-Guilbert
1Department of Clinical Hematology, Institute of Cancerology and Hematology, CHU Morvan, Avenue Foch, 29609 Brest, France.
Abstract:
We report here two cases of patients with acute myeloblastic leukemia, type M1 (FAB classification), associated with a t(10;17)(p15;q21). Fluorescence in situ hybridization with the LSI PML/RARA dual-color probe showed the breakpoint to be distal to the RARA locus. Four other patients with this translocation have been reported, three of them having acute undifferentiated or poorly differentiated leukemia.
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Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
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Translation Produces the Building Blocks of Life
Transposons

