Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

Jongmans, M.Kuiper, R.Carmichael, C.Wilkins, E.Dors, N.Carmagnac, A.Schouten-van Meeteren, N.Li, X.Stankovic, M.Kamping, E.Bengtsson, H.Schoenmakers, M.Geurts van Kessel, A.Hoogerbrugge, P.Hahn, C.Brons, P.Scott, H.Hoogerbrugge, N.2011-01-112011-01-112010Leukemia, 2010; 24(1):242-2460887-69241476-5551http://hdl.handle.net/2440/62193en© 2010 Nature Publishing GroupHumansBlood Platelet DisordersGene DeletionMutationChildChild, PreschoolFemaleMaleCore Binding Factor Alpha 2 SubunitLeukemia, Myeloid, AcuteNovel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndromeJournal article002009402210.1038/leu.2009.2100002735771000402-s2.0-7424910416836607Hahn, C. [0000-0001-5105-2554]Scott, H. [0000-0002-5813-631X]