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AML1-MTG16 fusion gene in therapy-related acute leukemia with t(16;21)(q24;q22); two new cases

✍ Scribed by Salomon-Nguyen, F; Busson-Le Coniat, M; Lafage Pochitaloff, M; Mozziconacci, J; Berger, R; Bernard, O A


Book ID
110054659
Publisher
Nature Publishing Group
Year
2000
Tongue
English
Weight
89 KB
Volume
14
Category
Article
ISSN
0887-6924

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## Abstract The t(1;21)(p36;q22) is a recurrent chromosome abnormality associated with therapy‐related acute myeloid leukemia (AML). Although involvement of __RUNX1__ has been detected by fluorescence in situ hybridization analysis, the partner gene has not been reported previously. We identified a