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Recurrently affected genes in juvenile myelomonocytic leukaemia
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Heterogeneous cytogenetic subgroups and outcomes in childhood acute megakaryoblastic leukemia: a retrospective international study
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Clinical impact of additional cytogenetic aberrations, cKIT and RAS mutations, and treatment elements in pediatric t(8;21)-AML : results from an international retrospective study by the International Berlin-Frankfurt-Münster study group
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Somatic genetic and epigenetic architecture of myelodysplastic syndromes arising from GATA2 deficiency
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IER3 expression in childhood myelodysplastic syndrome
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Integrated transcript and genome analyses reveal NKX2-1 and MEF2C as potential oncogenes in T cell acute lymphoblastic leukemia
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Molecular-genetic insights in paediatric T-cell acute lymphoblastic leukaemia
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- Journal Article
- A1
- open access
Leukemia-associated NF1 inactivation in patients with pediatric T-ALL and AML lacking evidence for neurofibromatosis
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The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia
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Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia