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Displaying 12 results.
    • Journal article
    Mutation screening in 18 Caucasian families suggest the existence of other MODY genes.
    Chèvre, J C Hani, E H Boutin, P Vaxillaire, M Blanché, H Vionnet, N Pardini, V C Timsit, J Larger, E Charpentier, G Beckers, Dominique[UCL] Maes, M Bellanné-Chantelot, C Velho, G Froguel, P (1998) Diabetologia — Vol. 41, no. 9, p. 1017-23 (1998)
    • Journal article
    del(7q) in chronic B-cell lymphoid malignancies
    Hernandez, Jesús María Mecucci, Cristina Michaux, Lucienne[UCL] Criel, Arnold Stul, Michel Meeus, Peter Wlodarska, Iwona Van Orshoven, Angeline Cassiman, Jean-Jacques De Wolf-Peeters, Christiane Van den Berghe, Herman (1997) Cancer Genetics and Cytogenetics — Vol. 93, no.2, p. 147-151 (1997)
    • Journal article
    Clonal monosomy 7 and 5q--in a child with myelodysplastic syndrome.
    Chantrain, Christophe[UCL] Vermylen, Christiane[UCL] Michaux, Lucienne[UCL] Brichard, Bénédicte[UCL] Cornu, Guy[UCL] (2000) Pediatric hematology and oncology — Vol. 17, no. 6, p. 505-9 (2000)
    • Journal article
    Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients.
    Vergult, Sarah Hoogeboom, A Jeannette M Bijlsma, Emilia K Sante, Tom Klopocki, Eva De Wilde, Bram Jongmans, Marjolijn Thiel, Christian Verheij, Joke B G M Perez-Aytes, Antonio Van Esch, Hilde Kuechler, Alma Barge-Schaapveld, Daniela Q C M Sznajer, Yves[UCL] Mortier, Geert Menten, Björn (2013) Genetics in Medicine — Vol. 15, no.3, p. 195-202 (2013)
    • Journal article
    Therapy-related acute myeloid leukemia in a child with Noonan syndrome and clonal duplication of the germline PTPN11 mutation.
    Chantrain, Christophe[UCL] Jijon, Priscilla[UCL] De Raedt, Thomas[UCL] Vermylen, Christiane[UCL] Poirel, Hélène[UCL] Legius, Eric[UCL] Brichard, Bénédicte[UCL] (2007) Pediatric Blood & Cancer — Vol. 48, no. 1, p. 101-104 (2007)
    • Journal article
    Localization of candidate regions for a novel gene for Kartagener syndrome.
    Gutierrez-Roelens, Ilse[UCL] Sluysmans, Thierry[UCL] Jorissen, Mark Amyere, Mustapha[UCL] Vikkula, Miikka[UCL] (2006) European Journal of Human Genetics — Vol. 14, no. 7, p. 809-815 (2006)
    • Journal article
    The impact of concomitant cytogenetic abnormalities on acute myeloid leukemia with monosomy 7 or deletion 7q after HLA-matched allogeneic stem cell transplantation.
    Poire, Xavier[UCL] Labopin, Myriam Polge, Emmanuelle Volin, Liisa Finke, Jürgen Ganser, Arnold Blaise, Didier Yakoub-Agha, Ibrahim Beelen, Dietrich Forcade, Edouard Lioure, Bruno Socié, Gérard Niederwieser, Dietger Labussière-Wallet, Hélène Maertens, Johan Cornelissen, Jan Craddock, Charles Mohty, Mohamad Esteve, Jordi Nagler, Arnon (2020) American journal of hematology — Vol. 95, no.3, p. 282-294 (2020)
    • Journal article
    Phosphoserine phosphatase deficiency in a patient with Williams syndrome
    Jaeken, Jaak Detheux, Michel Fryns, Jean-Pierre Collet, Jean-François[UCL] Alliet, Philippe Van Schaftingen, Emile[UCL] (1997) Journal of Medical Genetics — Vol. 34, no. 7, p. 594-596 (1997)
    • Journal article
    Myelodysplastic syndrome with monosomy 5 and/or 7 following therapy with 2-chloro-2'-deoxyadenosine.
    Van Den Neste, Eric[UCL] Louviaux, I Michaux, Jean-Louis[UCL] Delannoy, André[UCL] Michaux, Lucienne[UCL] Hagemeijer, Anne[UCL] Scheiff, Jean-Marie[UCL] Bosly, André[UCL] Straetmans, Nicole[UCL] Ferrant, Augustin[UCL] (1999) British journal of haematology — Vol. 105, no. 1, p. 268-70 (1999)
    • Journal article
    Mutation screening in 18 Caucasian families suggest the existence of other MODY genes
    Chevre, JC Maes, Marc[UCL] Hani, EH Boutin, P Vaxillaire, M. Blanche, H Vionnet, N. Pardini, VC Timsit, J Larger, E Charpentier, G. Beckers, D. Bellanne-Chantelot, C Velho, G. Froguel, P. (1998) Diabetologia : clinical and experimental diabetes and metabolism — Vol. 41, no. 9, p. 1017-23 (1998)
    • Journal article
    Integrative genomic and transcriptomic analysis identified candidate genes implicated in the pathogenesis of hepatosplenic T-cell lymphoma
    Finalet Ferreiro, Julio Rouhigharabaei, Leila Urbankova, Helena van der Krogt, Jo-Anne Michaux, Lucienne[UCL] Shetty, Shashirekha Krenacs, Laszlo Tousseyn, Thomas De Paepe, Pascale Uyttebroeck, Anne Verhoef, Gregor Taghon, Tom Vandenberghe, Peter Cools, Jan Wlodarska, Iwona (2014) PLoS One — Vol. 9, no.7, p. e102977 (2014)
    • Journal article
    3-Phosphoglycerate dehydrogenase deficiency and 3-phosphoserine phosphatase deficiency: inborn errors of serine biosynthesis.
    Jaeken, J Detheux, M Van Maldergem, L Frijns, J P Alliet, P Foulon, M Carchon, H Van Schaftingen, Emile[UCL] (1996) Journal of Inherited Metabolic Disease — Vol. 19, no.2, p. 223-6 (1996)