Authors: Marcelis, C Schrander-Stumpel, C Engelen, J Schoonbrood-Lenssen, A Willemse, A Beemer, F Sigaudy, S Missirian, C Philip, N Fryns, JP

Citation: C. Marcelis et al., Wolf-Hirschhorn (4p) syndrome in adults, GEN COUNSEL, 12(1), 2001, pp. 35-48

Authors: Bignell, GR Warren, W Seal, S Takahashi, M Rapley, E Barfoot, R Green, H Brown, C Biggs, PJ Lakhani, SR Jones, C Hansen, J Blair, E Hofmann, B Siebert, R Turner, G Evans, DG Schrander-Stumpel, C Beemer, FA van den Ouweland, A Halley, D Delpech, B Cleveland, MG Leigh, I Leisti, J Rasmussen, S Wallace, MR Fenske, C Banerjee, P Oiso, N Chaggar, R Merrett, S Leonard, N Huber, M Hohl, D Chapman, P Burn, J Swift, S Smith, A Ashworth, A Stratton, MR

Citation: Gr. Bignell et al., Identification of the familial cylindromatosis tumour-suppressor gene, NAT GENET, 25(2), 2000, pp. 160-165

Authors: Veugelers, M De Cat, B Muyldermans, SY Reekmans, G Delande, N Frints, S Legius, E Fryns, JP Schrander-Stumpel, C Weidle, B Magdalena, N David, G

Citation: M. Veugelers et al., Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene, HUM MOL GEN, 9(9), 2000, pp. 1321-1328

Authors: Takahashi, M Rapley, E Biggs, PJ Lakhani, SR Cooke, D Hansen, J Blair, E Hofmann, B Siebert, R Turner, G Evans, DG Schrander-Stumpel, C Beemer, FA van Vloten, WA Breuning, MH van den Ouweland, A Halley, D Delpech, B Cleveland, M Leigh, I Chapman, P Burn, J Hohl, D Gorog, JP Seal, S Mangion, J Warren, W Bignell, G Stratton, MR

Citation: M. Takahashi et al., Linkage and LOH studies in 19 cylindromatosis families show no evidence ofgenetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13, HUM GENET, 106(1), 2000, pp. 58-65

Authors: Schrander-Stumpel, C

Citation: C. Schrander-stumpel, Preconception care: Challenge of the new millennium?, AM J MED G, 89(2), 1999, pp. 58-61