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Full Text	Issue Date	Title	Author(s)
	2011	Diagnostiek bij multipel myeloom: de rol van beeldvorming, chromosomenanalyse en multiparameterflowcytometrie.	Zweegman, S.; Minnema, M.C.; Stevens-Kroef, M.J.P.L.; Kersten, M.J.; Wijermans, P.; Wegman, J.J.; Regelink, J.C.; Brooimans, R.A.; Beverloo, B.; Bloem, A.C.; Lokhorst, H.M.; Sonneveld, P.; Raymakers, R.A.P.
	2011	TET2 mutations in childhood leukemia	Langemeijer, S.M.C.; Jansen, J.H.; Hooijer, J.; Hoogen, P.C.M. van; Stevens-Linders, E.H.P.; Massop, M.; Waanders, E.; Reijmersdal, S.V. van; Stevens-Kroef, M.J.P.L.; Zwaan, C.M.; Heuvel-Eibrink, M.M. van den; Sonneveld, E.; Hoogerbrugge, P.M.; Geurts van Kessel, A.H.M.; Kuiper, R.P.
	2011	High prevalence of adverse prognostic genetic aberrations and unmutated IGHV genes in small lymphocytic lymphoma as compared to chronic lymphocytic leukemia.	Groenen, P.J.T.A.; Raymakers, R.; Rombout, P.D.M.; Prenter, M. de; Kossen, L.; Philipsen-Jansen, C.; Feuth, T.; Meijer, J.W.R.; Geurts van Kessel, A.H.M.; Krieken, J.H.J.M. van; Stevens-Kroef, M.J.P.L.
	2011	Microarray-based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia	Simons, A.; Stevens-Kroef, M.J.P.L.; El Idrissi-Zaynoun, N.; Gessel, S. van; Weghuis, D.O.; Berg, E. van den; Waanders, E.; Hoogerbrugge, P.M.; Kuiper, R.P.; Geurts van Kessel, A.H.M.
	2010	Gene expression profiling for molecular classification of multiple myeloma in newly diagnosed patients.	Broyl, A.; Hose, D.; Lokhorst, H.; Knegt, Y. de; Peeters, J.; Jauch, A.; Bertsch, U.; Buijs, A.; Stevens-Kroef, M.J.P.L.; Beverloo, H.B.; Vellenga, E.; Zweegman, S.; Kersten, M.J.; Holt, B. van der; Jarari, L. el; Mulligan, G.; Goldschmidt, H.; Duin, M. van; Sonneveld, P.
	2009	Heterogeneous patterns of amplification of the NUP214-ABL1 fusion gene in T-cell acute lymphoblastic leukemia.	Graux, C.; Stevens-Kroef, M.J.P.L.; Lafage, M.; Dastugue, N.; Harrison, C.J.; Mugneret, F.; Bahloula, K.; Struski, S.; Gregoire, M.J.; Nadal, N.; Lippert, E.; Taviaux, S.; Simons, A.; Kuiper, R.P.; Moorman, A.V.; Barber, K.; Bosly, A.; Michaux, L.; Berghe, P. van den; Lahortiga, I.; Keersmaecker, K. De; Wlodarska, I.; Cools, J.; Hagemeijer, A.; Poirel, H.A.
	2009	Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification.	Stevens-Kroef, M.J.P.L.; Simons, A.; Gorissen, H.; Feuth, A.B.; Weghuis, D.O.; Buijs, A.J.; Raymakers, R.A.P.; Geurts van Kessel, A.H.M.
	2006	Identification of truncated RUNX1 and RUNX1-PRDM16 fusion transcripts in a case of t(1;21)(p36;q22)-positive therapy-related AML.	Stevens-Kroef, M.J.P.L.; Schoenmakers, E.F.P.M.; Kraaij, M.G.J. van; Huys, E.; Vermeulen, S.; Reijden, B.A. van der; Geurts van Kessel, A.H.M.
	2004	Hypotriploidy 68,XX: a new case report and review of earlier cases.	Hoedemaekers, Y.M.; Kleine, M.J. de; Kroef, M.J.P.L.; Smeets, E.E.; Schrander-Stumpel, C.T.R.M.
	2004	Translocation t(2;3)(p15-23;q26-27) in myeloid malignancies: report of 21 new cases, clinical, cytogenetic and molecular genetic features.	Kroef, M.J.P.L.; Poppe, B.; Zelderen-Bhola, S. van; Berg, E. van den; Blij-Philipsen, M. van der; Geurts van Kessel, A.H.M.; Slater, R.; Hamers, G.J.; Michaux, L.; Speleman, F.; Hagemeijer, A.
	1997	Mosaicism of the 5q deletion as assessed by interphase FISH is a common phenomenon in MDS and restricted to myeloid cells	Kroef, M.J.P.L.; Bolk, M.J.W.; Muus, P.; Wessels, J.M.C.; Beverstock, G.C.; Willemze, R.; Landegent, J.E.

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