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CBFB-MYH11
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Identification of Fusion Gene Breakpoints is Feasible and Facilitates Accurate Sensitive Minimal Residual Disease Monitoring on Genomic Level in Patients With PML-RARA, CBFB-MYH11, and RUNX1-RUNX1T1
2020 |
Second Faculty of Medicine
publication
CBFB-MYH11 hypomethylation signature and PBX3 differential methylation revealed by targeted bisulfite sequencing in patients with acute myeloid leukemia
2014 |
First Faculty of Medicine
publication
Detection of fusion genes at the protein level in leukemia patients via the flow cytometric immunobead assay
2010 |
Second Faculty of Medicine