RUNX1 DNA-binding mutations and RUNX1-PRDM16 cryptic fusions in BCR-ABL+ leukemias are frequently associated with secondary trisomy 21 and may contribute to clonal evolution and imatinib resistance

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Title
RUNX1 DNA-binding mutations and RUNX1-PRDM16 cryptic fusions in BCR-ABL+ leukemias are frequently associated with secondary trisomy 21 and may contribute to clonal evolution and imatinib resistance
Authors
Keywords
-
Journal
BLOOD
Volume 111, Issue 7, Pages 3735-3741
Publisher
American Society of Hematology
Online
2008-01-18
DOI
10.1182/blood-2007-07-102533

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