论文信息 - A rare case of acute megakaryoblastic leukemia with t(11;17)(q23;q21) and KMT2A::MLLT6 fusion - 字舞流文

A rare case of acute megakaryoblastic leukemia with t(11;17)(q23;q21) and KMT2A::MLLT6 fusion

L. Medeiros | Sa A. Wang | B. Thakral | G. Tang | Lianqun Qiu | C. Nunez | G. Issa | Branko Cuglievan

[1] C. Harrison,et al. Cytogenetics of Pediatric Acute Myeloid Leukemia: A Review of the Current Knowledge , 2021, Genes.

[2] Marilyn M. Li,et al. Clinical impact of genomic characterization of 15 patients with acute megakaryoblastic leukemia–related malignancies , 2021, Cold Spring Harbor molecular case studies.

[3] E. Clappier,et al. The MLL recombinome of acute leukemias in 2017 , 2017, Leukemia.

[4] Heather L. Mulder,et al. Pediatric non–Down syndrome acute megakaryoblastic leukemia is characterized by distinct genomic subsets with varying outcomes , 2017, Nature Genetics.

[5] M. Fornerod,et al. Recurrent abnormalities can be used for risk group stratification in pediatric AMKL: a retrospective intergroup study. , 2016, Blood.

[6] R. Danis,et al. A Review of Current Knowledge , 2017 .