Articles

P35 In-house developed 15-gene sequencing panel for acute myeloid leukemia and myelodysplasia allows robust detection of genetic defects including FLT3-ITD and CEBPA mutations

BJH - volume 8, issue Abstract Book BHS, february 2017

B. Denys MD, J. Van der Meulen , E. de Latter , S. Lefever , T. Rosseel , W. Steyaert , G. Vandercruyssen , I. Rottiers , D. Creytens , dr. J. Van Dorpe , F. Speleman PhD, B. Poppe , N. Van Roy PhD, K. de Leeneer , K. Claes , K. Vandepoele PhD

Read more

P.02 H3K27me3 erasers, novel targets in T-cell acute lymphoblastic leukaemia

BJH - 2013, issue BHS Abstractbook, january 2013

J. Van der Meulen , K. Mavrakis , V. Sanghvi , B. Poppe , N. Van Roy PhD, P. Rondou , Y Benoit MD, PhD, P. Van Vlierberghe PhD, H. Wendel , F. Speleman PhD

Read more

P.03 Extending the functional redundant cooperative miRNA tumour suppressor and oncogene network in T-ALL

BJH - 2013, issue BHS Abstractbook, january 2013

E. Mets , G. van Peer , J. Van der Meulen , P. Mestdagh , T. Taghon , D. Avran , Y Benoit MD, PhD, B. Poppe , J. Soulier , P. Van Vlierberghe PhD, P. Rondou , J. Vandesompele , F. Speleman PhD

Read more

P.37 Incidental diagnosis of Fanconi anemia in an adult patient with myelodysplastic syndrome

BJH - 2013, issue BHS Abstractbook, january 2013

B. Poppe , E. Steel , S. Callens MD, PhD, K. Bonte , A. d’Heedene , F. Speleman PhD, B. Menten , N. Van Roy PhD

Read more
X