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All Publications

Displaying 4 results.
    • Journal article
    Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease
    Beyens, G. Van Hul, E. Van Driessche, K. Fransen, E. Devogelaer, Jean-Pierre[UCL] Vanhoenacker, F. Van Offel, J. Verbruggen, L. De Clerck, L. Westhovens, R. Van Hul, W. (2004) Calcified Tissue International — Vol. 75, no. 2, p. 144-152 (2004)
    • Speech
    Genetic variation in the TNFRSF11A (RANK) gene contributes to the risk to develop sporadic Paget's disease of bone
    Chung, P. Y. J. Devogelaer, Jean-Pierre[UCL] Beyens, G. Riches, P. L. Van Wesenbeeck, L. Jennes, K. Daroszewska, A. Boonen, S.[UCL] Geusens, R. Vanhoenacker, F. Verbruggen, L. Van Offel, J. Goemaere, S. Zmierczak, H. Westhovens, Rene[UCL] Karperien, M. Papapoulos, S. Ralston, S. H. Van Hul, W. (2009) 36th European Symposium on Calcified Tissues — Vienna (Austria)
    • Speech
    Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion
    Wuyts, W. Roland, D. Ludecke, HJ Wauters, J. Foulon, Michel[UCL] Van Hul, W. Van Maldergem, L. (2002) 49th Annual Meeting of the American-Society-of-Human-Genetics — SAN FRANCISCO(California)
    • Speech
    Camurati-Engelmann disease is caused by mutations in the TGFB1 gene
    Janssens, K Gershoni-Baruch, R Guanabens, N Migone, N. Ralston, SH MacPherson, H Bonduelle, M. Lissens, W. Van Maldergem, L. Vanhoenacker, F. Verbruggen, L. Van Hul, W. (2001) —