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Results: 1-6 |
Results: 6

Authors: Brekelmans, CTM Seynaeve, C Bartels, CCM Tilanus-Linthorst, MMA Meijers-Heijboer, EJ Crepin, CMG van Geel, AN Menke, M Verhoog, LC van den Ouweland, A Obdeijn, IM Klijn, JGM
Citation: Ctm. Brekelmans et al., Effectiveness of breast cancer surveillance in BRCA1/2 gene mutation carriers and women with high familial risk, J CL ONCOL, 19(4), 2001, pp. 924-930

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: 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: Dabora, SL Nieto, AA Franz, D Jozwiak, S van den Ouweland, A Kwiatkowski, D
Citation: Sl. Dabora et al., Characterisation of six large deletions in TSC2 identified using long range PCR suggests diverse mechanisms including Alu mediated recombination, J MED GENET, 37(11), 2000, pp. 877-882

Authors: Shugart, YY Cour, C Renard, H Lenoir, G Goldgar, D Teare, D Easton, D Rahman, N Gusterton, R Seal, S Barfoot, R Stratton, M Mangion, J Peelen, T van den Ouweland, A Meijers, H Devilee, P Eccles, D Lynch, H Weber, B Stoppa-Lyonnet, D Bignon, YJ
Citation: Yy. Shugart et al., Linkage analysis of 56 multiplex families excludes the Cowden disease genePTEN as a major contributor to familial breast cancer, J MED GENET, 36(9), 1999, pp. 720-721

Authors: van Slegtenhorst, M Verhoef, S Tempelaars, A Bakker, L Wang, Q Wessels, M Bakker, R Nellist, M Lindhout, D Halley, D van den Ouweland, A
Citation: M. Van Slegtenhorst et al., Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosiscomplex patients: no evidence for genotype-phenotype correlation, J MED GENET, 36(4), 1999, pp. 285-289
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