View Author
cancer breast mutation carrier brca 1 genetic university study breast cancer department breast cancer risk center research association institute genetics service hospital analysis centre allele service genet oncology sample stage mutation carriers haplotype medicine population rhamm women netherland table figure brca 2 mutations genotype variant foundation cancer risk control model health aurka region per-allele susceptibility estimate family italy grant depletion result polarization disease france brca 2 stage 1 america evidence genome-wide association study germany erasmus universiteit rotterdam state individual brca 2 carriers ashkenazi diagnosis ratio genotyping genotyped chromosome receptor antoniou cancer institute centrosome ptrend program brca 1 carriers downloaded expression
7 Most Recent Publications
|
Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer
(Article)
Maxwell, C.A. Benitez, J. Mohan, P. Buys, S.S. John, E.M. Miron, A. Southey, M.C. Daly, M. Schmutzler, R.K. Wappenschmidt, B. Meindl, A. Arnold, N. Deissler, H. Català, I. Varon-Mateeva, R. Sutter, C. Niederacher, D. Imyamitov, E. Sinilnikova, O. Stoppa-Lyonne, D. Mazoyer, S. Verny-Pierre, C. Castera, L. Pauw, A. de Petit, A. Bignon, Y.-J. Uhrhammer, N. Peyrat, J.-P. Vennin, P. Ferrer, S.F. Collonge-Rame, M.-A. Mortemousque, I. Spurdle, A.B. Beesley, J. Healey, S. Aguilar, H. Barcellos-Hoff, M.H. Vidal, M. Gruber, S.B. Lazaro, C. Capellá, G. McGuffog, L. Nathanson, K.L. Antoniou, A.C. Chenevix-Trench, G. Fleisch, M.C. Villanueva, A. Moreno, V. Pujana, M.A. Aytes, A. Serra-Musach, J. Rennert, G. Lejbkowicz, F. Peterlongo, P. Gómez-Baldó, L. Manoukian, S. Peissel, B. Ripamonti, C.B. Bonanni, B. Viel, A. Allavena, A. Bernard, L. Radice, P. Friedman, E. Kaufman, B. Osorio, A. Laitman, Y. Dubrovsky, M. Milgrom, R. Jakubowska, A. Cybulski, C. Górski, B. Jaworska, K. Durda, K. Sukiennicki, G. Lubinski, J. Bonifaci, N. Shugart, Y.Y. Domchek, S.M. Letrero, R. Weber, B.L. Hogervorst, F.B.L. Rookus, M.A. Collée, J.M. Devilee, P. Ligtenberg, M. Luijt, R.B. van der Fernández-Ramires, R. Aalfs, C. Waisfisz, Q. Wijnen, J.T. Roozendaal, C.E.P. van Easton, D.F. Peock, S. Cook, J. Oliver, C. Frost, D. Harrington, P. Costes, S.V. Lalloo, F. Eeles, R. Izatt, L. Chu, C. Eccles, D. Douglas, F. Brewer, C. Nevanlinna, H. Heikinen, T. Couch, F.J. Guinó, E. Lindor, N.M. Wang, X. Godwin, A.K. Caligo, M.A. Lombardi, G. Loman, N. Karlsson, P. Ehrencrona, H. Wachenfeldt, A. von Barkardottir, R.B. Chen, H. Hamann, U. Rashid, M.U. Lasa, A. Caldes, T. Andres, R. Schmitt, M. Assmann, V. Stevens, K. Offit, K. Curado, J. Evans, G.J.R. Tilgner, H. Guigó, R. Aiza, G. Brunet, J. Castellsagué, J. Martrat, G. Urruticoechea, A. Blanco, I. Tihomirova, L. Goldgar, D. |
2011-11-01
|
|
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
(Article)
Antoniou, A.C. kartsonaki, C. Zaffaroni, D. Hopper, J. Daly, M. Terry, M-B. John, E.M. Buys, S.S. Yassin, Y. Miron, A. Goldgar, D. Singer, C.F. Tea, M.-K. Cattaneo, E. Pfeiler, G. Dressler, C. Hansen, T.V.O. Jønson, L. Ejlertsen, B. Barkardottir, R.B. Kirchhoff, T. Offit, K. Piedmonte, M. Rodriguez, G.C. Barile, M. Small, L. Boggess, J.F. Blank, S.V. Basil, J. Azodi, M. Toland, A.E. Montagna, M. Tognazzo, S. Agata, S. Imyanitov, E.N. Pensotti, V. Janavicius, R. Lazaro, C. Blanco, I. Pharoah, P.D.P. Sucheston, L. Karlan, B.Y. Walsh, C.S. Olah, E. Bozsik, A. Teo, S.-H. Pasini, B. Seldon, J.L. Beattie, M.S. Rensburg, E.J. van Sluiter, M.D. Diez, O. Schmutzler, R.K. Wappenschmidt, B. Engel, C. Meindl, A. Ruehl, I. Dolcetti, R. Varon-Mateeva, R. Kast, K. Deissler, H. Niederacher, D. Arnold, N. Gadzicki, D. Schönbuchner, I. Caldes, T. Hoya, M. de La Nevanlinna, H. Giannini, G. Aittomäki, K. Dumont, M. Chiquette, J. Tischkowitz, M. Chenevix-Trench, G. Beesley, J. Spurdle, A.B. Neuhausen, S.L. Ding, Y.C. Fredericksen, Z. Putignano, A.L. Wang, X. Pankratz, V.S. Couch, F.J. Simard, J. Easton, D.F. Chenevix-Trench, G. Karlsson, P. Nordling, M. Bergman, A. Einbeigi, Z. Varesco, L. Stenmark-Askmalm, M. Liedgren, S. Borg, A. Olsson, H. Kristoffersson, U. Jernström, H. Henriksson, K. Wachenfeldt, A. von Liljegren, A. Barbany-Bustinza, G. Radice, P. Rantala, J. Grönberg, H. Stattin, E.-L. Emanuelsson, M. Brandell, R.R. Dahl, N. Verhoef, S. Verheus, M. Veer, L.v. Leeuwen, F.E. van Sinilnikova, O. Mai, P.L. Collee, J.M. Ouweland, A.M.W. van den Jager, A. Tilanus-Linthorst, M.M.A. Seynaeve, C.M. Wijnen, J.T. Vreeswijk, M.P. Tollenaar, R.A.E.M. Ligtenberg, M. Hoogerbrugge, N. Greene, M.H. Ausems, M.G.E.M. Aalfs, C. Gille, J.J.P. Waisfisz, Q. Gómez García, E.B. Roozendaal, C.E. van Blok, M.J. Caanen, B. Oosterwijk, J.C. Hout, A.H. van der Andrulis, I.L. Mourits, M.J. Vasen, H.F. Gregory, H. Morrison, P.J. Jeffers, L. Cole, T.J. McKeown, C. Hoffman, J. Donaldson, A. Downing, S. Glendon, G. Taylor, A. Murray, A. Rogers, M.T. McCann, E. Barton, D. Porteous, M.E. Drummond, S. Brewer, C. Kivuva, E. Searle, A. Ozcelik, H. Goodman, S. Hill, K. Murday, V. Bradshaw, N. Snadden, L. Longmuir, M. Watt, C. Gibson, S. Haque, E. Tobias, E. Thomassen, M. Duncan, A. Jacobs, C. Langman, C. Whaite, A. Dorkins, H. Barwell, J. Chu, C. Miller, J. Ellis, I.O. Houghton, C. Gerdes, A-M. Side, L. Male, A. Berlin, C. Eason, J. Collier, R. Claber, O. Jobson, I. Walker, L. McLeod, D. Halliday, D. Kruse, T.A. Durell, S. Stayner, B. Shanley, S. Rahman, N. Houlston, R. Bancroft, E. D'Mello, L. Page, E. Ardern-Jones, A. Kohut, K. Jensen, U.B. Wiggins, J. Castro, E. Mitra, A. Robertson, L. Quarrell, O. Bardsley, C. Hodgson, S.V. Goff, S. Brice, G. Winchester, L. Cruger, D. Eddy, C. Tripathi, V. Attard, V. Lucassen, A. Crawford, G. McBride, D. Smalley, S. Adlard, J.W. Arver, B. Soucy, P. Caligo, M.A. Laitman, Y. Milgrom, R. Kaufman, B. Paluch-Shimon, S. Friedman, E. Loman, N. Harbst, K. Lindblom, A. Ehrencrona, H. McGuffog, L. Melin, B. Nathanson, K.L. Domchek, S.M. Rebbeck, T.R. Jakubowska, A. Lubinski, J. Gronwald, J. Huzarski, T. Byrski, T. Cybulski, C. Healey, S. Górski, B. Osorio, A. Cajal, T.R. Fostira, F. Andres, R. Benitez, J. Hamann, U. Hogervorst, F.B.L. Rookus, M.A. Hooning, M. Lee, A. Nelen, M.R. Luijt, R.B. van der Os, T.A.M. van Asperen, C.J. van Devilee, P. Meijers-Heijboer, H. Garcia, E.B.G. Peock, S. Cook, M. Frost, D. Peterlongo, P. Platte, R. Leyland, J. Evans, D.G. Lalloo, F. Eeles, R. Izatt, L. Davidson, R. Eccles, D. Ong, K.-R. Douglas, F. Manoukian, S. Paterson, J. Kennedy, M.J. Miedzybrodzka, Z. Godwin, A.K. Stoppa-Lyonnet, D. Buecher, B. Belotti, M. Tirapo, C. Mazoyer, S. Barjhoux, L. Peissel, B. Lassett, C. Leroux, D. Faivre, L. Bronner, M. Prieur, F. Nogues, C. Rouleau, E. Pujol, P. Coupier, I. Frenay, M. |
2011-08-01
|
|
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers
(Article)
Im, K.M. Kirchhoff, T. Guiducci, C. Vénat-Bouvet, L. Stoppa-Lyonnet, D. Chenevix-Trench, G. Easton, D.F. Klein, R.J. Friedman, E. Dean, M. Clark, A.G. Altshuler, D. Antoniou, A.C. Crenshaw, A. Couch, F.J. Offit, K. Gold, B. McGuffog, L. kartsonaki, C. Morrison, J. Healey, S. Sinilnikova, O. Mai, P.L. Greene, M.H. Piedmonte, M. Wang, X. Rubinstein, W.S. Hogervorst, F.B.L. Rookus, M.A. Collée, J.M. Hoogerbrugge, N. Asperen, C.J. van Meijers-Heijboer, H. Roozendaal, C.E. van Caldes, T. Perez-Segura, P. Green, T. Jakubowska, A. Lubinski, J. Huzarski, T. Blecharz, P. Nevanlinna, H. Aittomäki, K. Lazaro, C. Blanco, I. Barkardottir, R.B. Montagna, M. Chow, C.Y. D'Andrea, E. Devilee, P. Olopade, O.I. Neuhausen, S.L. Peissel, B. Bonanni, B. Peterlongo, P. Singer, C.F. Rennert, G. Lejbkowicz, F. Vijai, J. Andrulis, I.L. Glendon, G. Ozcelik, H. Toland, A.E. Caligo, M.A. Beattie, M.S. Chan, S. Domchek, S.M. Nathanson, K.L. Rebbeck, T.R. Korn, J.M. Phelan, C. Narod, S. John, E.M. Hopper, J. Buys, S.S. Daly, M. Southey, M.C. Terry, M-B. Tung, N. Hansen, T.V.O. Gaudet, M.M. Osorio, A. Benitez, J. Durán, M. Weitzel, J.N. Garber, J. Hamann, U. Peock, S. Cook, J. Oliver, C. Frost, D. Fredericksen, Z. Platte, R. Evans, D.G. Eeles, R. Izatt, L. Paterson, J. Brewer, C. Hodgson, S.V. Porteous, M.E. Walker, L. Rogers, M.T. Shane Pankratz, V. Side, L. Godwin, A.K. Schmutzler, R.K. Wappenschmidt, B. Laitman, Y. Meindl, A. Deissler, H. Varon-Mateeva, R. Preisler-Adams, S. Kast, K. |
2011-05-20
|
|
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
(Article)
Ramus, S.J. kartsonaki, C. Wang, X. Collonge-Rame, M.-A. Vénat-Bouvet, L. Fert-Ferrer, S. Miron, A. Buys, S.S. Hopper, J. Daly, M. John, E.M. Terry, M-B. Goldgar, D. Fredericksen, Z. Hansen, T.V.O. Jønson, L. Ejlertsen, B. Agnarsson, B.A. Offit, K. Kirchhoff, T. Vijai, J. Dutra-Clarke, A. Przybylo, J.A. Montagna, M. Peterlongo, P. Casella, C. Imyanitov, E.N. Janavicius, R. Blanco, I. Lazaro, C. Moysich, K.B. Karlan, B.Y. Gross, J. Beattie, M.S. Schmutzler, R.K. Manoukian, S. Wappenschmidt, B. Meindl, A. Ruehl, I. Fiebig, B. Sutter, C. Arnold, N. Deissler, H. Varon-Mateeva, R. Kast, K. Niederacher, D. Peissel, B. Gadzicki, D. Caldes, T. Hoya, M. de La Nevanlinna, H. Aittomäki, K. Simard, J. Soucy, P. Spurdle, A.B. Holland, H. Easton, D.F. Zaffaroni, D. Antoniou, A.C. Asperen, C.J. van Roversi, G. Barile, M. Viel, A. Allavena, A. Gayther, S.A. Ottini, L. Papi, L. Gismondi, V. Capra, F. Radice, P. Greene, M.H. Mai, P.L. Andrulis, I.L. Glendon, G. Ozcelik, H. Pharoah, P.D.P. Thomassen, M. Gerdes, A-M. Kruse, T.A. Cruger, D. Jensen, U.B. Caligo, M.A. Olsson, H. Kristoffersson, U. Lindblom, A. Arver, B. Sinilnikova, O. Karlsson, P. Stenmark-Askmalm, M. Borg, A. Neuhausen, S.L. Ding, Y.C. Nathanson, K.L. Domchek, S.M. Jakubowska, A. Lubinski, J. Huzarski, T. Beesley, J. Byrski, T. Gronwald, J. Górski, B. Cybulski, C. Dbniak, T. Osorio, A. Durán, M. Tejada, M.-I. Benitez, J. Hamann, U. Chenevix-Trench, G. Rookus, M.A. Verhoef, S. Tilanus-Linthorst, M.A. Vreeswijk, M.P. Bodmer, D. Ausems, M.G.E.M. Os, T.A.M. van Blok, M.J. Meijers-Heijboer, H. Peock, S. McGuffog, L. Cook, J. Oliver, C. Frost, D. Dunning, A.M. Evans, D.G. Eeles, R. Pichert, G. Cole, T.J. Hodgson, S.V. Brewer, C. Healey, S. Morrison, P.J. Porteous, M.E. Kennedy, M.J. Rogers, M.T. Side, L. Donaldson, A. Gregory, H. Godwin, A.K. Stoppa-Lyonnet, D. Moncoutier, V. Couch, F.J. Castera, L. Mazoyer, S. Barjhoux, L. Bonadona, V. Leroux, D. Faivre, L. Lidereau, R. Nogues, C. Bignon, Y.-J. Prieur, F. |
2011-01-19
|
|
Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: Implications for risk prediction
(Article)
Antoniou, A.C. Beesley, J. Isaacs, C. Bonadona, V. Lassett, C. Dreyfus, H. Leroux, D. Hardouin, A. Berthet, P. Faivre, L. Loustalot, C. Noguchi, T. Sobol, H. Ganz, P.A. Rouleau, E. Nogues, C. Frenay, M. Vénat-Bouvet, L. Hopper, J. Daly, M. Terry, M-B. John, E.M. Buys, S.S. Yassin, Y. Tomlinson, G. Miron, A. Goldgar, D. Singer, C.F. Dressler, C. Gschwantler-Kaulich, D. Pfeiler, G. Hansen, T.V.O. Jnson, L. Agnarsson, B.A. Kirchhoff, T. Olopade, O.I. Offit, K. Devlin, V. Dutra-Clarke, A. Piedmonte, M. Rodriguez, G.C. Wakeley, K. Boggess, J.F. Basil, J. Schwartz, P.E. Blank, S.V. Couch, F.J. Toland, A.E. Montagna, M. Casella, C. Imyanitov, E.N. Tihomirova, L. Blanco, I. Lazaro, C. Ramus, S.J. Sucheston, L. Karlan, B.Y. Wang, X. Gross, J. Schmutzler, R.K. Wappenschmidt, B. Engel, C. Meindl, A. Lochmann, M. Arnold, N. Heidemann, S. Varon-Mateeva, R. Niederacher, D. Lindor, N.M. Sutter, C. Deissler, H. Gadzicki, D. Preisler-Adams, S. Kast, K. Schönbuchner, I. Caldes, T. Hoya, M. de La Aittomäki, K. Nevanlinna, H. Pankratz, V.S. Simard, J. Spurdle, A.B. Holland, H. Chenevix-Trench, G. Platte, R. Easton, D.F. Radice, P. Manoukian, S. McGuffog, L. Peissel, B. Zaffaroni, D. Barile, M. Viel, A. Allavena, A. Dall'Olio, V. Peterlongo, P. Szabo, C. Zikan, M. Claes, K. Sinilnikova, O. Poppe, B. Foretova, L. Mai, P.L. Greene, M.H. Rennert, G. Lejbkowicz, F. Glendon, G. Ozcelik, H. Andrulis, I.L. Thomassen, M. Healey, S. Gerdes, A-M. Sunde, L. Cruger, D. Jensen, U.B. Caligo, M.A. Friedman, E. Kaufman, B. Laitman, Y. Milgrom, R. Dubrovsky, M. Neuhausen, S.L. Cohen, S. Borg, A. Jernström, H. Lindblom, A. Rantala, J. Stenmark-Askmalm, M. Melin, B. Nathanson, K.L. Domchek, S.M. Jakubowska, A. Ding, Y.C. Lubinski, J. Huzarski, T. Osorio, A. Lasa, A. Durán, M. Tejada, M.I. Godino, J. Benitez, J. Hamann, U. Kriege, M. Rebbeck, T.R. Hoogerbrugge, N. Luijt, R.B. van der Asperen, C.J. van Devilee, P. Meijers-Heijboer, E.J. Blok, M.J. Aalfs, C. Hogervorst, F.B.L. Rookus, M.A. Cook, J. Weitzel, J. Oliver, C. Frost, D. Conroy, D. Evans, D.G. Lalloo, F. Pichert, G. Davidson, R. Cole, T.J. Paterson, J. Hodgson, S.V. Lynch, H. Morrison, P.J. Porteous, M.E. Walker, L. Kennedy, M.J. Dorkins, H. Peock, S. Godwin, A.K. Stoppa-Lyonnet, D. Pauw, A. de Mazoyer, S. |
2010-12-01
|
|
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
(Article)
Antoniou, A.C. Wang, X. Ghoussaini, M. Caldes, T. Hoya, M. de La Singer, C.F. Fink-Retter, A. Greene, M.H. Mai, P.L. Loud, J.T. Guidugli, L. Lindor, N.M. Hansen, T.V.O. Barrowdale, D. Nielsen, F.C. Blanco, I. Lazaro, C. Garber, J. Ramus, S.J. Gayther, S.A. Phelan, C. Narod, S. Szabo, C. Benitez, J. Peock, S. Osorio, A. Nevanlinna, H. Heikkinen, T. Caligo, M.A. Beattie, M.S. Hamman, U. Godwin, A.K. Montagna, M. Casella, C. Neuhausen, S.L. Cook, M. Karlan, B.Y. Tung, N. Toland, A.E. Weitzel, J. Olopade, P. Simard, J. Soucy, P. Rubinstein, W.S. Arason, A. Rennert, G. Oliver, C. Martin, N.G. Montgomery, G.W. Chang-Claude, J. Flesch-Janys, D. Brauch, H. Severi, G. Baglietto, L. Cox, A. Cross, S.S. Miron, P. Frost, D. Gerty, S.M. Tapper, W. Yannoukakos, D. Fountzilas, G. Fasching, P.A. Beckmann, M.W. Dos Santos Silva, I. Peto, J. Lambrechts, D. Paridaens, R. Eccles, D. Rüdiger, T. Försti, A. Winqvist, R. Pylkäs, K. Diasio, R.B. Lee, A.M. Eckel-Passow, J. Vachon, C. Blows, F. Driver, K. Evans, D.G. Dunning, A.M. Pharaoh, P.D.P. Offit, K. Pankratz, V.S. Hakonarson, H. Chenevix-Trench, G. Easton, D.F. Couch, F.J. Eeles, R. Izatt, L. Fredericksen, Z. Chu, C. Douglas, F. Paterson, J. Stoppa-Lyonnet, D. Houdayer, C. Mazoyer, S. Giraud, S. Lassett, C. Remenieras, A. Caron, O. McGuffog, L. Hardouin, A. Berthet, P. Hogervorst, F.B.L. Rookus, M.A. Jager, A. Ouweland, A.M.W. van den Hoogerbrugge, N. Luijt, R.B. van der Meijers-Heijboer, H. G'mez García, E.B. Tarrell, R. Devilee, P. Vreeswijk, M.P. Lubinski, J. Jakubowska, A. Gronwald, J. Huzarski, T. Byrski, T. G'rski, B. Cybulski, C. Spurdle, A.B. Sinilnikova, O. Holland, H. Goldgar, D. John, E.M. Hopper, J. Southey, M.C. Buys, S.S. Daly, M.B. Terry, M-B. Schmutzler, R.K. Wappenschmidt, B. Healey, S. Engel, C. Meindl, A. Preisler-Adams, S. Arnold, N. Niederacher, D. Sutter, C. Domchek, S.M. Nathanson, K.L. Rebbeck, T.R. Blum, J.L. Morrison, J. Piedmonte, M. Rodriguez, G.C. Wakeley, K. Boggess, J.F. Basil, J. Blank, S.V. Friedman, E. Kaufman, B. Laitman, Y. Milgrom, R. kartsonaki, C. Andrulis, I.L. Glendon, G. Ozcelik, H. Kirchhoff, T. Vijai, J. Gaudet, M.M. Altshuler, D. Guiducci, C. Loman, N. Harbst, K. Lesnick, T. Rantala, J. Ehrencona, H. Gerdes, A-M. Thomassen, M. Sunde, L. Peterlongo, P. Manoukian, S. Bonanni, B. Viel, A. Radice, P. |
2010-10-01
|
|
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer
(Article)
Gaudet, M.M. Kirchhoff, T. Morrison, J. Godwin, A.K. Schmutzler, R.K. Wappenschmidt, B. Engert, S. Arnold, N. Gadzicki, D. Dean, M. Gold, B. Klein, R.J. Couch, F.J. Healey, S. Chenevix-Trench, G. Easton, D.F. Daly, M. Antoniou, A.C. Altshuler, D. Offit, K. Sinilnikova, O. Stoppa-Lyonnet, D. Mazoyer, S. Gauthier-Villars, M. Sobol, H. Longy, M. Frenay, M. Hogervorst, F.B.L. Green, T. Rookus, M.A. Collée, J.M. Hoogerbrugge, N. Roozendaal, K.E. van Piedemonte, M. Rubinstein, W.S. Nerenstone, S. Le, L. van Blank, S.V. Caldes, T. Vijai, J. Hoya, M. de La Nevanlinna, H. Aittomäki, K. Lazaro, C. Blanco, I. Arason, A. Johannsson, O.T. Barkardottir, R.B. Devilee, P. Olopade, O.I. Korn, J.M. Neuhausen, S.L. Wang, X. Fredericksen, Z. Peterlongo, P. Manoukian, S. Barile, M. Viel, A. Radice, P. Phelan, C. Narod, S. Guiducci, C. Rennert, G. Lejbkowicz, F. Flugelman, A. Andrulis, I.L. Glendon, G. Ozcelik, H. Toland, A.E. Montagna, M. D'Andrea, E. Friedman, E. Segrè, A.V. Laitman, Y. Borg, A. Beattie, M.S. Ramus, S.J. Domchek, S.M. Nathanson, K.L. Rebbeck, T.R. Spurdle, A.B. Chen, X. Holland, H. McGee, K. John, E.M. Hopper, J. Buys, S.S. Daly, M.B. Southey, M.C. Terry, M-B. Tung, N. Hansen, T.V.O. Nielsen, F.C. Greene, M.H. McGuffog, L. Mai, P.L. Osorio, A. Duran, M. Andres, R. Benítez, J. Weitzel, J. Garber, J. Hamann, U. Peock, S. Cook, M. kartsonaki, C. Oliver, C. Frost, D. Platte, R. Evans, D.G. Lalloo, F. Eeles, R. Izatt, L. Walker, L. Eason, J. Barwell, J. |
2010-10-01
|