Associated Papers
Molecular characterization of AML with RUNX1-RUNX1T1 at diagnosis and relapse reveals net loss of co-mutations.
Höllein A et al.
Hemasphere, 2019
31723813 (PubMed )
Supplement: hs9-3-e178-s001.pdf
Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations.
Micol JB et al.
Blood, 2014
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