Results: 1-5 |
Results: 5

Authors: Tavtigian, SV Simard, J Teng, DHF Abtin, V Baumgard, M Beck, A Camp, NJ Carillo, AR Chen, Y Dayananth, P Desrochers, M Dumont, M Farnham, JM Frank, D Frye, C Ghaffari, S Gupte, JS Hu, R Iliev, D Janecki, T Kort, EN Laity, KE Leavitt, A Leblanc, G McArthur-Morrison, J Pederson, A Penn, B Peterson, KT Reid, JE Richards, S Schroeder, M Smith, R Snyder, SC Swedlund, B Swensen, J Thomas, A Tranchant, M Woodland, AM Labrie, F Skolnick, MH Neuhausen, S Rommens, J Cannon-Albright, LA
Citation: Sv. Tavtigian et al., A candidate prostate cancer susceptibility gene at chromosome 17p, NAT GENET, 27(2), 2001, pp. 172-180

Authors: Alos, N Moisan, AM Ward, L Desrochers, M Legault, L Leboeuf, G Van Vliet, G Simard, J
Citation: N. Alos et al., A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3 beta-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians: Evaluation of gonadal function after puberty, J CLIN END, 85(5), 2000, pp. 1968-1974

Authors: Mazoyer, S Leary, J Kirk, J Fleischmann, E Wagner, T Claes, K Messiaen, L Foulkes, W Desrochers, M Simard, J Phelan, CM Kwan, E Narod, SA Vahteristo, P Nevanlinna, H Durando, X Bignon, YJ Peyrat, JP Bonnardel, C Sinilnikova, OM Puget, N Lenoir, GM Mazoyer, S Audoynaud, C Goldgar, D Maugard, C Caux, V Gad, S Stoppa-Lyonnet, D Nogues, C Lidereau, R Machavoine, C Bressac-de Paillerets, B Kuschel, B Betz, B Niederacher, D Beckmann, MW Hamann, U Gayther, SA Ponder, BAP Robinson, M Taylor, GR Bishop, T Catteau, A Solomon, E Cohen, B Steel, M Collins, N Stratton, M van der Looij, M Olah, E Miller, NJ Barton, DE Sverdlov, RS Friedman, E Radice, P Montagna, M Sensi, E Caligo, M van Eijk, R Devilee, P van der Luijt, R Heimdal, K Moller, P Borg, A Diez, O Cortes, J Domenech, M Baiget, M Osorio, A Benitez, J Borg, A Maillet, P Sappino, AP Ozdag, H Ozcelik, T Ozturk, M Rohlfs, EM Boyd, J McDermott, D Offit, K Unger, M Nathanson, K Weber, BL Sellers, TA Hampton, E Couch, FJ Neuhausen, S
Citation: S. Mazoyer et al., The exon 13 duplication in the BRCA1 gene is a founder mutation present ingeographically diverse populations, AM J HU GEN, 67(1), 2000, pp. 207-212

Authors: Desrochers, M Jones, CV Lenstra, JK Savelsbergh, MWP Stougie, L
Citation: M. Desrochers et al., Towards a model and algorithm management system for vehicle routing and scheduling problems, DECIS SUP S, 25(2), 1999, pp. 109-133

Authors: Moisan, AM Ricketts, ML Tardy, V Desrochers, M Mebarki, F Chaussain, JL Cabrol, S Raux-Demay, MC Forest, MG Sippell, WG Peter, M Morel, Y Simard, J
Citation: Am. Moisan et al., Commentary - New insight into the molecular basis of 3 beta-hydroxysteroiddehydrogenase deficiency: Identification of fight mutations in the HSD3B2 gene in eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes, J CLIN END, 84(12), 1999, pp. 4410-4425
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