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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

W. Van Hul

Department of Medical Genetics

University of Antwerp



Name/email consistency: high



  • Department of Medical Genetics, University of Antwerp, Belgium. 1997 - 1998


  1. 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) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
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