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Displaying 9 results.
    • Journal article
    Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Francais de Cytogenetique Hematologique
    Jeandidier, E Michaux, Lucienne[UCL] Dastugue, N. Mugneret, Francine Lafage-Pochitaloff, M. Mozziconacci, Marie-Joëlle Herens, C. Dumoulin, Christine[UCL] Talmant, P. Cornillet-Lefebvre, P. Luquet, I. Charrin, C. Barin, C. Collonge-Rame, MA Perot, C. Van den Akker, J. Gregoire, MJ Jonveaux, P. Baranger, L. Eclache-Saudreau, V Pages, MP. Cabrol, C. Terre, C. Berger, R. (2006) Cancer Genetics and Cytogenetics — Vol. 166, no. 1, p. 1-11 (2006)
    • Journal article
    Trisomy 20q - a New Case and Further Phenotypic Delineation
    Herens, C. Verloes, A. Laloux, F. Vanmaldergem, L. (1990) Clinical Genetics : an international journal of genetics and molecular medicine — Vol. 37, no. 5, p. 363-366 (1990)
    • Journal article
    Expression analyses identify MLL as a prominent target of 11q23 amplification and support an etiologic role for MLL gain of function in myeloid malignancies
    Poppe, B. Vandesompele, J. Schoch, C Lindvall, C Mrozek, K Bloomfield, CD Beverloo, HB Michaux, Lucienne[UCL] Dastugue, N. Herens, C. Yigit, N De Paepe, A. Hagemeijer, Anne[UCL] Speleman, F. (2004) Blood — Vol. 103, no. 1, p. 229-235 (2004)
    • Journal article
    PAX5/IGH rearrangement is a recurrent finding in a subset of aggressive B-NHL with complex chromosomal rearrangements
    Poppe, B. De Paepe, P Michaux, Lucienne[UCL] Dastugue, N. Bastard, C. Herens, C. Moreau, E Cavazzini, F[UCL] Yigit, N Van Limbergen, H De Paepe, A. Praet, M De Wolf-Peeters, C. Wlodarska, Iwona[UCL] Speleman, F. (2005) Genes, Chromosomes & Cancer — Vol. 44, no. 2, p. 218-223 (2005)
    • Journal article
    Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH
    Van Limbergen, H Michaux, Lucienne[UCL] Poppe, B. Herens, C. Brown, J. Noens, L. Berneman, Z. De Bock, R De Paepe, A. Speleman, F. (2002) Genes, Chromosomes & Cancer — Vol. 33, no. 1, p. 60-72 (2002)
    • Journal article
    Roberts-sc Phocomelia Syndrome With Exencephaly
    Verloes, A. Herens, C. Vanmaldergem, L. Retz, MC. Dodinval, P. (1989) Annales de génétique — Vol. 32, no. 3, p. 169-170 (1989)
    • Speech
    Amplification of chromosome 11q23 involving the MLL gene is recurrently observed in myeloid leukemias.
    Michaux, Lucienne[UCL] Dierlamm, J. Stul, M. Wlodarska, Iwona[UCL] Herens, C. Beverloo, B Duhem, C Lecomte, M. Verhoef, G. Dumoulin, Christine[UCL] Hagemeijer, Anne[UCL] (1998) —
    • Speech
    Report of 38 patients with hyperdiploid karyotype in acute myeloid leukemia: A groupe francais de cytogenetique hematologique study
    Terre, C. Luquet, I. Laie, J. L. Barin, C. Baranger, L. Bilhou-Nabera, C. Lippert, E. Gervais, C. Talmant, P. Cornillet-Lefebvre, P. Perot, C. Nadal, N. Mozziconacci, Marie-Joëlle Lafage-Pochitaloff, M. Eclache, V. Mugneret, Francine Lefebvre, Chantal[UCL] Herens, C. Speleman, F. Poirel, Hélène Tigaud, I. Cabrol, C. Rousselot, P. Castaigne, S. Berger, R. (2007) 12th Congress of the European-Hematology-Association — Vienna (Austria)
    • Journal article
    MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23
    Michaux, Lucienne[UCL] Ferrant, Augustin[UCL] Wlodarska, Iwona[UCL] Stul, M. Dierlamm, J. Mugneret, Francine Herens, C. Beverloo, B Verhest, A. Dumoulin, Christine[UCL] Verhoef, G. Selleslag, M Madoe, V Lecomte, M. Deprijck, B. Delannoy, André[UCL] Marichal, S. Duhem, C Dicato, M. Hagemeijer, Anne[UCL] (2000) Genes, Chromosomes & Cancer — Vol. 29, no. 1, p. 40-47 (2000)