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Displaying 3 results.
    • Journal article
    Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
    Pansuriya, Twinkal C van Eijk, Ronald d'Adamo, Pio van Ruler, Maayke A J H Kuijjer, Marieke L Oosting, Jan Cleton-Jansen, Anne-Marie van Oosterwijk, Jolieke G Verbeke, Sofie L J Meijer, Daniëlle van Wezel, Tom Nord, Karolin H Sangiorgi, Luca Toker, Berkin Liegl-Atzwanger, Bernadette San-Julian, Mikel Sciot, Raf Limaye, Nisha[UCL] Kindblom, Lars-Gunnar Daugaard, Soeren Godfraind, Catherine[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] Kurek, Kyle C Szuhai, Karoly French, Pim J Bovée, Judith V M G (2011) Nature Genetics — Vol. 43, no. 12, p. 1256-61 (2011)
    • Journal article
    PTHR1 mutations associated with Ollier disease result in receptor loss of function
    Couvineau, Alain Wouters, Vinciane[UCL] Bertrand, Guylène Rouyer, Christiane Gérard, Bénédicte Boon, Laurence M.[UCL] Grandchamp, Bernard Vikkula, Miikka[UCL] Silve, Caroline (2008) Human Molecular Genetics — Vol. 17, no. 18, p. 2766-75 (2008)
    • Journal article
    Sporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2.
    Ghalamkarpour, Arash Debauche, Christian[UCL] Haan, Eric Van Regemorter, Nicole Sznajer, Yves Thomas, Dominique Revencu, Nicole Gillerot, Yves Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2009) The Journal of pediatrics — Vol. 155, no. 1, p. 90-3 (2009)