Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21.

af 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
Udgivet 1998

Polymorphisms in the Low-Density Lipoprotein Receptor-Related Protein 5 (LRP5) Gene Are Associated with Peak Bone Mass in Non-sedentary Men: Results from the Odense Androgen Study

af Brixen, K., Beckers, S., Peeters, A., Piters, E., Balemans, W., Nielsen, T. L., Wraae, K., Bathum, L., Brasen, C., Hagen, C., Andersen, M., Van Hul, W., Abrahamsen, B.
Udgivet 2007

Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease

af Balemans, W, Patel, N, Ebeling, M, Van Hul, E, Wuyts, W, Lacza, C, Dioszegi, M, Dikkers, F, Hildering, P, Willems, P, Verheij, J, Lindpaintner, K, Vickery, B, Foernzler, D, Van Hul, W
Udgivet 2002

Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21.

af Balemans, W, Van Den Ende, J, Freire Paes-Alves, A, Dikkers, F G, Willems, P J, Vanhoenacker, F, de Almeida-Melo, N, Alves, C F, Stratakis, C A, Hill, S C, Van Hul, W
Udgivet 1999

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

af Verhoeven, K, Van Camp, G, Govaerts, P J, Balemans, W, Schatteman, I, Verstreken, M, Van Laer, L, Smith, R J, Brown, M R, Van de Heyning, P H, Somers, T, Offeciers, F E, Willems, P J
Udgivet 1997