Wim Wuyts
Department of Medical Genetics
University of Antwerp
Belgium
Name/email consistency: high
- Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects. Wuyts, W., Waeber, G., Meinecke, P., Schüler, H., Goecke, T.O., Van Hul, W., Bartsch, O. Eur. J. Hum. Genet. (2004)
- Molecular basis of multiple exostoses: mutations in the EXT1 and EXT2 genes. Wuyts, W., Van Hul, W. Hum. Mutat. (2000)
- Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna. Wuyts, W., Reardon, W., Preis, S., Homfray, T., Rasore-Quartino, A., Christians, H., Willems, P.J., Van Hul, W. Hum. Mol. Genet. (2000)
- Characterization and genomic localization of the mouse Extl2 gene. Wuyts, W., Van Hul, W. Cytogenet. Cell Genet. (2000)
- The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). Wuyts, W., Cleiren, E., Homfray, T., Rasore-Quartino, A., Vanhoenacker, F., Van Hul, W. J. Med. Genet. (2000)
- Molecular and clinical examination of an Italian DEFECT11 family. Wuyts, W., Di Gennaro, G., Bianco, F., Wauters, J., Morocutti, C., Pierelli, F., Bossuyt, P., Van Hul, W., Casali, C. Eur. J. Hum. Genet. (1999)
- Refined physical mapping and genomic structure of the EXTL1 gene. Wuyts, W., Spieker, N., Van Roy, N., De Boulle, K., De Paepe, A., Willems, P.J., Van Hul, W., Versteeg, R., Speleman, F. Cytogenet. Cell Genet. (1999)
