W. Van Hul
Department of Medical Genetics
University of Antwerp
Belgium
Name/email consistency: high
- Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21. Van Hul, W., Balemans, W., Van Hul, E., Dikkers, F.G., Obee, H., Stokroos, R.J., Hildering, P., Vanhoenacker, F., Van Camp, G., Willems, P.J. Am. J. Hum. Genet. (1998)
- Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene family. Van Hul, W., Wuyts, W., Hendrickx, J., Speleman, F., Wauters, J., De Boulle, K., Van Roy, N., Bossuyt, P., Willems, P.J. Genomics (1998)
- Localization of a gene for autosomal dominant osteopetrosis (Albers-Schönberg disease) to chromosome 1p21. Van Hul, W., Bollerslev, J., Gram, J., Van Hul, E., Wuyts, W., Benichou, O., Vanhoenacker, F., Willems, P.J. Am. J. Hum. Genet. (1997)