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Nature Genetics|January 1, 1993
A point mutation in the FMR-1 gene associated with fragile X mental retardationK De Boulle, A J Verkerk, E Reyniers, et al.American Journal of Medical Genetics|August 9, 1996
Transgenic mouse model for the fragile X syndromeR F Kooy, R D'Hooge, E Reyniers, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|July 11, 2001
Melanoma screening: results of the first one-day campaign in Belgium ('melanoma Monday')M M Vandaele, B Richert, J D Van der Endt, et al.American Journal of Human Genetics|April 16, 1998
Mutations in the EXT1 and EXT2 genes in hereditary multiple exostosesW Wuyts, W Van Hul, K De Boulle, et al.Human Molecular Genetics|October 1, 1996
Positional cloning of a gene involved in hereditary multiple exostosesW Wuyts, W Van Hul, J Wauters, et al.Pageof 3