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A novel four-way t(6;16;21;8)(p21.3;p11.2;q22;q22) in acute myeloid leukemia with RUNX1/RUNX1T1 rearrangement

✍ Scribed by Kyoung-Jin Park; Hyung-Doo Park; Hee-Jin Kim; Keon Hee Yoo; Hong Hoe Koo; Sun-Hee Kim

Book ID
113513546
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
365 KB
Volume
192
Category
Article
ISSN
0165-4608

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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