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A novel RUNX1-C11orf41 fusion gene in a case of acute myeloid leukemia with a t(11;21)(p14;q22)

✍ Scribed by Akihiro Abe; Akira Katsumi; Miki Kobayashi; Akinao Okamoto; Masutaka Tokuda; Tadaharu Kanie; Yukiya Yamamoto; Tomoki Naoe; Nobuhiko Emi


Book ID
119211560
Publisher
Elsevier
Year
2012
Tongue
English
Weight
233 KB
Volume
205
Category
Article
ISSN
2210-7762

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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