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Menten, B, Maas, N, Thienpont, B, Buysse, K, Vandesompele, J, Melotte, C, de Ravel, T, Van Vooren, S, Balikova, I, Backx, L, Janssens, S, De Paepe, A, De Moor, B, Moreau, Y, Marynen, P, Fryns, J-P, Mortier, G, Devriendt, K, Speleman, F, Vermeesch, J R
Published in Journal of medical genetics (01.08.2006)
Published in Journal of medical genetics (01.08.2006)
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Published in The New England journal of medicine (27.03.2003)
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Role of cardiac myocyte tissue factor in heart hemostasis
PAWLINSKI, R., TENCATI, M., HOLSCHER, T., PEDERSEN, B., VOET, T., TILLEY, R. E., MARYNEN, P., MACKMAN, N.
Published in Journal of thrombosis and haemostasis (01.08.2007)
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FOXP1, a gene highly expressed in a subset of diffuse large B-cell lymphoma, is recurrently targeted by genomic aberrations
WLODARSKA, I, VEYT, E, DE WOLF-PEETERS, C, DE PAEPE, P, VANDENBERGHE, P, NOOIJEN, P, THEATE, I, MICHAUX, L, SAGAERT, X, MARYNEN, P, HAGEMEIJER, A
Published in Leukemia (01.08.2005)
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Clinical and molecular features of FIP1L1-PDFGRA (+) chronic eosinophilic leukemias
VANDENBERGHE, P, WLODARSKA, I, MAEREVOET, M, VERHOEF, G, COOLS, J, GILLILAND, D. G, HAGEMEIJER, A, MARYNEN, P, MICHAUX, L, ZACHEE, P, BOOGAERTS, M, VANSTRAELEN, D, HERREGODS, M-C, VAN HOOF, A, SELLESLAG, D, ROUFOSSE, F
Published in Leukemia (01.04.2004)
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A new recurrent inversion, inv(7)(p15q34), leads to transcriptional activation of HOXA10 and HOXA11 in a subset of T-cell acute lymphoblastic leukemias
SPELEMAN, F, CAUWELIER, B, BOOGAERTS, M, DE MOERLOOSE, B, BENOIT, Y, SELLESLAG, D, BILLIET, J, ROBERT, A, HUGUET, F, VANDENBERGHE, P, DE PAEPE, A, MARYNEN, P, DASTUGUE, N, HAGEMEIJER, A, COOLS, J, VERHASSELT, B, POPPE, B, VAN ROY, N, VANDESOMPELE, J, GRAUX, C, UYTTEBROECK, A
Published in Leukemia (01.03.2005)
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Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map
Van Buggenhout, G, Melotte, C, Dutta, B, Froyen, G, Van Hummelen, P, Marynen, P, Matthijs, G, de Ravel, T, Devriendt, K, Fryns, J P, Vermeesch, J R
Published in Journal of medical genetics (01.09.2004)
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Novel PORCN mutations in focal dermal hypoplasia
Froyen, G, Govaerts, K, Van Esch, H, Verbeeck, J, Tuomi, M-L, Heikkilä, H, Torniainen, S, Devriendt, K, Fryns, J-P, Marynen, P, Järvelä, I, Ala-Mello, S
Published in Clinical genetics (01.12.2009)
Published in Clinical genetics (01.12.2009)
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Translocations t(11;18)(q21;q21) and t(14;18)(q32;q21) are the main chromosomal abnormalities involving MLT/MALT1 in MALT lymphomas
PENAS, E. M, HINZ, K, DIERLAMM, J, RÖSER, K, COPIE-BERGMAN, C, WLODARSKA, I, MARYNEN, P, HAGEMEIJER, A, GAULARD, P, LÖNING, T, HOSSIELD, D. K
Published in Leukemia (01.11.2003)
Published in Leukemia (01.11.2003)
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Interstitial del(14)(q) involving IGH: a novel recurrent aberration in B-NHL
Pospisilova, H, Baens, M, Michaux, L, Stul, M, Van Hummelen, P, Van Loo, P, Vermeesch, J, Jarosova, M, Zemanova, Z, Michalova, K, Van den Berghe, I, Alexander, H D, Hagemeijer, A, Vandenberghe, P, Cools, J, De Wolf-Peeters, C, Marynen, P, Wlodarska, I
Published in Leukemia (01.09.2007)
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A new NDE1 PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome
La Starza, R, Rosati, R, Roti, G, Gorello, P, Bardi, A, Crescenzi, B, Pierini, V, Calabrese, O, Baens, M, Folens, C, Cools, J, Marynen, P, Martelli, M F, Mecucci, C, Cuneo, A
Published in Leukemia (01.04.2007)
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CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients
La Starza, R, Aventin, A, Crescenzi, B, Gorello, P, Specchia, G, Cuneo, A, Angioni, A, Bilhou-Nabera, C, Boqué, C, Foà, R, Uyttebroeck, A, Talmant, P, Cimino, G, Martelli, M F, Marynen, P, Mecucci, C, Hagemeijer, A
Published in Leukemia (01.09.2005)
Published in Leukemia (01.09.2005)
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Transition from EML1-ABL1 to NUP214-ABL1 positivity in a patient with acute T-lymphoblastic leukemia
DE KEERSMAECKER, K, LAHORTIGA, I, GRAUX, C, MARYNEN, P, MAERTENS, J, COOLS, J, VANDENBERGHE, P
Published in Leukemia (01.12.2006)
Published in Leukemia (01.12.2006)
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Detection of t(11;18)(q21;q21) by interphase fluorescence in situ hybridization using API2 and MLT specific probes
DIERLAMM, Judith, BAENS, Mathijs, HAGEMEIJER, Anne, HOSSFELD, Dieter Kurt, DE WOLF-PEETERS, Christiane, MARYNEN, Peter, STEFANOVA-OUZOUNOVA, Margarita, HINZ, Kristina, WLODARSKA, Iwona, MAES, Brigitte, STEYLS, Anja, DRIESSEN, Ann, VERHOEF, Gregor, GAULARD, Philippe
Published in Blood (15.09.2000)
Published in Blood (15.09.2000)
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FIP1L1-PDGFRA in chronic eosinophilic leukemia and BCR-ABL1 in chronic myeloid leukemia affect different leukemic cells
CRESCENZI, B, CHASE, A, JONES, A. V, CROSS, N. C. P, MARYNEN, P, MECUCCI, C, LA STARZA, R, BEACCI, D, ROSTI, V, GALLI, A, SPECCHIA, G, MARTELLI, M. F, VANDENBERGHE, P, COOLS, J
Published in Leukemia (01.03.2007)
Published in Leukemia (01.03.2007)
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Detection and validation of copy number variation in X-linked mental retardation
Bauters, M., Weuts, A., Vandewalle, J., Nevelsteen, J., Marynen, P., Van Esch, H., Froyen, G.
Published in Cytogenetic and genome research (01.01.2008)
Published in Cytogenetic and genome research (01.01.2008)
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e6-a2 BCR-ABL1 fusion in T-cell acute lymphoblastic leukemia
Quentmeier, H, Cools, J, Macleod, R A F, Marynen, P, Uphoff, C C, Drexler, H G
Published in Leukemia (01.02.2005)
Published in Leukemia (01.02.2005)
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Translocation t(1;6)(p35.3;p25.2): a new recurrent aberration in 'unmutated' B-CLL
MICHAUX, L, WLODARSKA, I, VAN HOOF, A, FERRANT, A, MARYNEN, P, HAGEMEIJER, A, RACK, K, STUL, M, CRIEL, A, MAEREVOET, M, MARICHAL, S, DEMUYNCK, H, MINEUR, P, KARGAR SAMANI, K
Published in Leukemia (01.01.2005)
Published in Leukemia (01.01.2005)
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