Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer von Kar, Siddhartha, Jiang, Xia, Finucane, Hilary, McGuffog, Lesley, Adams, Marcia, Agata, Simona, Allen, Jamie, Bernstein, Leslie, Bobolis, Kristie, Bogdanova, Natalia V, Bozsik, Aniko, Brand, Judith S, Brauch, Hiltrud, Brenner, Hermann, Bressac-de Paillerets, Brigitte, Brinton, Louise, Cai, Qiuyin, Caligo, Maria A, Castelao, J Esteban, Castera, Laurent, Chanock, Stephen J, Christiansen, Hans, Diez, Orland, Domchek, Susan M, dos-Santos-Silva, Isabel, Eeles, Ros, Ehrencrona, Hans, Eilber, Ursula, Ekici, Arif B, Engel, Christoph, Flyger, Henrik, Ganz, Patricia A, Garber, Judy, Gerdes, Anne-Marie, Glendon, Gord, Godwin, Andrew K, Goldgar, David E, González-Neira, Anna, Goodfellow, Paul, Greene, Mark H, Alnæs, Grethe I Grenaker, Haeberle, Lothar, Hankinson, Susan, Hodgson, Shirley, Hu, Chunling, Hunter, David J, Jensen, Uffe Birk, Jones, Michael, Kabisch, Maria, Kerin, Michael J, Khan, Sofia, Knight, Julia A, Lecarpentier, Julie, Lilyquist, Jenna, Lincoln, Anne, Lindblom, Annika, Luccarini, Craig, MacInnis, Robert J, Maishman, Tom, Miller, Nicola, Nadesan, Sue, Neuhausen, Susan L, Nevelsteen, Ines, Nordestgaard, Børge G, Olopade, Olufunmilayo I, Peixoto, Ana, Peto, Julian, Prokofieva, Darya, Radice, Paolo, Rahman, Nazneen, Rennert, Gad, Romero, Atocha, Sanders, Joyce, Schmidt, Daniel F, Schoemaker, Minouk J, Schwentner, Lukas, Sheng, Xin, Sukiennicki, Grzegorz, Surowy, Harald, Sutter, Christian, Swerdlow, Anthony, Tan, Yen Y, Tibiletti, Maria Grazia, Tihomirova, Laima, Tong, Ling, Truong, Thérèse, Tyrer, Jonathan, van Rensburg, Elizabeth J, Weinberg, Clarice R, Whittemore, Alice S, Winqvist, Robert, Wolk, Alicja, Yang, Xiaohong R, Zheng, Wei, Ottini, Laura, Thomassen, Mads, Schmutzler, Rita K, Couch, Fergus J, García-Closas, Montserrat, Simard, Jacques

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Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers von Page, Elizabeth C., Bancroft, Elizabeth K., Brook, Mark N., Assel, Melissa, Hassan Al Battat, Mona, Thomas, Sarah, Taylor, Natalie, Raghallaigh, Holly Ni, Evans, D. Gareth, Maehle, Lovise, Grindedal, Eli Marie, James, Paul, Mascarenhas, Lyon, McKinley, Joanne, Thomas, Tessy, van Asperen, Christi, Vasen, Hans, Kiemeney, Lambertus A., Ringelberg, Janneke, Jensen, Thomas Dyrsø, Osther, Palle J.S., Helfand, Brian T., Genova, Elena, Oldenburg, Rogier A., Cybulski, Cezary, Ong, Kai-Ren, Lam, Jimmy, Taylor, Louise, Feliubadaló, Lidia, van Zelst-Stams, Wendy, Rosario, Derek J., Domchek, Susan, Powers, Jacquelyn, Buys, Saundra, O'Toole, Karen, Ausems, Margreet G.E.M., Schmutzler, Rita K., Rhiem, Kerstin, Izatt, Louise, Cardoso, Marta, Aprikian, Armen, van Randeraad, Heleen, Davidson, Rosemarie, Longmuir, Mark, Helderman van den Enden, Apollonia T.J.M., Adank, Muriel, Williams, Rachel, Andrews, Lesley, Murphy, Declan G., Halliday, Dorothy, Walker, Lisa, Liljegren, Annelie, Carlsson, Stefan, Morton, Catherine, Snape, Katie, Hanson, Helen, Tischkowitz, Marc, Taylor, Amy, Kirk, Judy, Susman, Rachel, Chen-Shtoyerman, Rakefet, Spigelman, Allan, Pachter, Nicholas, Ahmed, Munaza, Ramon y Cajal, Teresa, Brewer, Carole, Gadea, Neus, van Os, Theo, Gallagher, David, Johannsson, Oskar, Barwell, Julian, Nicolai, Nicola, Friedman, Eitan, Greenhalgh, Lynn, Murthy, Vedang, Saya, Sibel, McGrath, John, Rønlund, Karina, Teo, Soo H., Kast, Karin, Aaronson, Neil K., Ardern-Jones, Audrey, Bangma, Chris H., Dearnaley, David, Tricker, Karen, Eyfjord, Jorunn, Falconer, Alison, Foster, Christopher, Gronberg, Henrik, Hamdy, Freddie C., Stefansdottir, Vigdis, Khoo, Vincent, Lindeman, Geoffrey J., Lubinski, Jan, Mikropoulos, Christos, Mitra, Anita, Moynihan, Clare, Wilson, Penny, Dudderidge, Tim, Offman, Judith

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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants von Barnes, Daniel R., Rookus, Matti A., Dennis, Joe, Mavaddat, Nasim, Ahmed, Munaza, Aittomäki, Kristiina, Andrulis, Irene L., Arun, Banu K., Barkardottir, Rosa B., Barrowdale, Daniel, Benitez, Javier, Białkowska, Katarzyna, Blok, Marinus J., Bonanni, Bernardo, Bozsik, Aniko, Buys, Saundra S., Caldés, Trinidad, Campbell, Ian, Christensen, Lise Lotte, Colas, Chrystelle, Berthet, Pascaline, Faivre, Laurence, Giraud, Sophie, Lasset, Christine, Mebirouk, Noura, Adlard, Julian, Antoniou, Antonis, Brennan, Paul, Brewer, Carole, Cook, Jackie, Easton, Douglas, Eeles, Ros, Hanson, Helen, Izatt, Louise, Ong, Kai-ren, O’Shaughnessy-Kirwan, Aoife, Daly, Mary B., Davidson, Rosemarie, Ding, Yuan Chun, Dorfling, Cecilia M., Engel, Christoph, Evans, D. Gareth, Friedlander, Michael, Friedman, Eitan, Ganz, Patricia A., Gerdes, Anne-Marie, Giraud, Sophie, Glendon, Gord, Godwin, Andrew K., Gschwantler-Kaulich, Daphne, Hamann, Ute, Hu, Chunling, Hulick, Peter J., Hogervorst, Frans, Koudijs, Marco, Kruse, Torben A., Lazaro, Conxi, Lester, Jenny, Mai, Phuong L., Mari, Véronique, Meijers-Heijboer, Hanne E.J., Meindl, Alfons, Mensenkamp, Arjen R., Montagna, Marco, Mukherjee, Semanti, Mulligan, Anna Marie, Nevanlinna, Heli, Niederacher, Dieter, Olopade, Olufunmilayo I., Ott, Claus-Eric, Papi, Laura, Park, Sue K., Peissel, Bernard, Pfeiler, Georg, Phillips, Kelly-Anne, Prajzendanc, Karolina, Pujana, Miquel Angel, Ramus, Susan J., Rantala, Johanna, Rennert, Gad, Risch, Harvey A., Schuster, Hélène, Senter, Leigha, Side, Lucy E., Slavin, Thomas P., Soucy, Penny, Sutter, Christian, Thull, Darcy L., Toland, Amanda E., Tung, Nadine, van Engelen, Klaartje, van Rensburg, Elizabeth J., Wang-Gohrke, Shan, Wappenschmidt, Barbara, Yang, Xin, Zimbalatti, Dario, Offit, Kenneth, Couch, Fergus J., Schmutzler, Rita K., Antoniou, Antonis C.

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Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations von Bancroft, Elizabeth K., Saya, Sibel, Page, Elizabeth C., Myhill, Kathryn, Thomas, Sarah, Pope, Jennifer, Chamberlain, Anthony, Hart, Rachel, Glover, Wayne, Cook, Jackie, Rosario, Derek J., Helfand, Brian T., Hutten Selkirk, Christina, Davidson, Rosemarie, Longmuir, Mark, Eccles, Diana M., Gadea, Neus, Brewer, Carole, Barwell, Julian, Salinas, Monica, Greenhalgh, Lynn, Tischkowitz, Marc, Henderson, Alex, Evans, David Gareth, Buys, Saundra S., Eeles, Rosalind A., Aaronson, Neil K.

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Comprehensive cancer-predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes von Whitworth, J, Smith, PS, Martin, J-E, West, H, Luchetti, A, Rodger, F, Clark, G, Carss, K, Stephens, J, Stirrups, K, Penkett, C, Mapeta, R, Ashford, S, Megy, K, Shakeel, H, Ahmed, M, Adlard, J, Barwell, J, Brewer, C, Casey, RT, Armstrong, R, Cole, T, Evans, DG, Fostira, F, Greenhalgh, L, Hanson, H, Henderson, A, Hoffman, J, Izatt, L, Kumar, A, Kwong, A, Lalloo, F, Ong, KR, Paterson, J, Park, S-M, Chen-Shtoyerman, R, Searle, C, Side, L, Skytte, A-B, Snape, K, Woodward, ER, Tischkowitz, MD, Maher, ER

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Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer... von Soucy, Penny, Pastinen, Tomi, Droit, Arnaud, Arason, Adalgeir, Arun, Banu K., Azzollini, Jacopo, Bane, Anita, Barjhoux, Laure, Barrowdale, Daniel, Benitez, Javier, Berthet, Pascaline, Blok, Marinus J., Bonanni, Bernardo, Bradbury, Angela R., Buecher, Bruno, Buys, Saundra S., Chiquette, Jocelyne, Chung, Wendy K., Claes, Kathleen B. M., Daly, Mary B., Davidson, Rosemarie, De la Hoya, Miguel, De Leeneer, Kim, Dolcetti, Riccardo, Dorfling, Cecilia M., Eccles, Diana, Einbeigi, Zakaria, Engel, Christoph, Feliubadalo, Lidia, Foretova, Lenka, Fostira, Florentia, Fountzilas, George, Friedman, Eitan, Frost, Debra, Ganschow, Pamela, Garber, Judy, Gayther, Simon A., Greene, Mark H., Gronwald, Jacek, Hamann, Ute, Hart, Steven, Imyanitov, Evgeny N., Jakubowska, Anna, Janavicius, Ramunas, Jensen, Uffe Birk, John, Esther M., Joseph, Vijai, Just, Walter, Karlan, Beth Y., Kets, Carolien M., Kirk, Judy, Kriege, Mieke, Laurent, Maïté, Lazaro, Conxi, Lester, Jenny, Liljegren, Annelie, Loud, Jennifer T., Manoukian, Siranoush, Mariani, Milena, Meindl, Alfons, Montagna, Marco, Mulligan, Anna Marie, Neuhausen, Susan L., Nevanlinna, Heli, Nussbaum, Robert L., Olah, Edith, Olopade, Olufunmilayo I., Ong, Kai-ren, Oosterwijk, Jan C., Papi, Laura, Park, Sue Kyung, Pedersen, Inge Sokilde, Peterlongo, Paolo, Rantala, Johanna, Rappaport-Fuerhauser, Christine, Richardson, Andrea, Robson, Mark, Rookus, Matti A., Shah, Payal D., Slavin, Thomas P., Sokolowska, Johanna, Spurdle, Amanda B., Stadler, Zsofia, Tea, Muy-Kheng, Teulé, Alex, Terry, Mary Beth, Tihomirova, Laima, Tischkowitz, Marc, Tognazzo, Silvia, Toland, Amanda Ewart, Tung, Nadine, van den Ouweland, Ans M. W., van der Luijt, Rob B., van Engelen, Klaartje, Varon-Mateeva, Raymonda, Wijnen, Juul T., Rebbeck, Timothy, Chenevix-Trench, Georgia, Nord, Silje, Easton, Douglas F.

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Fine-scale mapping at 9p22.2 identifies candidate causal variants that modify ovarian cancer risk in BRCA1 and BRCA2 mutation carriers von Kuchenbaecker, KB, Beesley, J, Agnarsson, BA, Andrulis, IL, Barjhoux, L, Belotti, M, Bojesen, A, Brewer, C, Caldes, T, Campbell, I, Claes, Kathleen, Cohn, DE, Daly, MB, Davidson, R, Domchek, SM, Dumont, M, Durda, K, Dworniczak, B, Easton, DF, Eccles, D, Ardnor, CE, Eeles, R, Ejlertsen, B, Ellis, S, Evans, DG, Feliubadalo, L, Fostira, F, Foulkes, WD, Friedman, E, Frost, D, Gaddam, P, Garber, J, Garcia-Barberan, V, Gauthier-Villars, M, Gerdes, AM, Giraud, S, Goldgar, DE, Hake, CR, Healey, S, Hodgson, S, Houdayer, C, Hulick, PJ, Imyanitov, EN, Isaacs, C, Izatt, L, Jakubowska, A, Janavicius, R, Jaworska-Bieniek, K, John, EM, Vijai, J, Karlan, BY, Kast, K, Kwong, A, Laitman, Y, Lesueur, F, Liljegren, A, Manoukian, S, Meindl, A, Mensenkamp, AR, Montagna, M, Nathanson, KL, Neuhausen, SL, Nevanlinna, H, Olah, E, Ong, KR, Osorio, A, Pedersen, IS, Peissel, B, Pfeiler, G, Phelan, CM, Piedmonte, M, Poppe, Bruce, Radice, P, Rookus, MA, Ross, EA, Schmutzler, RK, Simard, J, Singer, CF, Slavin, TP, Stoppa-Lyonnet, D, Sukiennicki, G, Sutter, C, Szabo, CI, Teixeira, MR, Terry, MB, Thomassen, M, Tibiletti, MG, Tihomirova, L, Varon-Mateeva, R, Vratimos, A, Weitzel, JN, Toland, AE, Hamann, U, Lindor, N, Ramus, SJ, Greene, MH, Couch, FJ, Pharoah, PDP, Chenevix-Trench, G, Antoniou, AC

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Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers von Walker, Logan C, Fredericksen, Zachary S, Wang, Xianshu, Tarrell, Robert, Pankratz, Vernon S, Lindor, Noralane M, Beesley, Jonathan, Healey, Sue, Chen, Xiaoqing, Stoppa-Lyonnet, Dominique, Tirapo, Carole, Giraud, Sophie, Mazoyer, Sylvie, Muller, Danièle, Fricker, Jean-Pierre, Delnatte, Capucine, Schmutzler, Rita K, Wappenschmidt, Barbara, Engel, Christoph, Schönbuchner, Ines, Deissler, Helmut, Meindl, Alfons, Hogervorst, Frans B, Verheus, Martijn, Hooning, Maartje J, van den Ouweland, Ans Mw, Nelen, Marcel R, Ausems, Margreet Gem, Aalfs, Cora M, van Asperen, Christi J, Devilee, Peter, Gerrits, Monique M, Waisfisz, Quinten, Szabo, Csilla I, Easton, Douglas F, Peock, Susan, Cook, Margaret, Oliver, Clare T, Frost, Debra, Harrington, Patricia, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Chu, Carol, Davidson, Rosemarie, Eccles, Diana, Ong, Kai-Ren, Cook, Jackie, Rebbeck, Tim, Nathanson, Katherine L, Domchek, Susan M, Singer, Christian F, Gschwantler-Kaulich, Daphne, Dressler, Anne-Catharina, Pfeiler, Georg, Godwin, Andrew K, Heikkinen, Tuomas, Nevanlinna, Heli, Agnarsson, Bjarni A, Caligo, Maria Adelaide, Olsson, Håkan, Kristoffersson, Ulf, Liljegren, Annelie, Arver, Brita, Karlsson, Per, Melin, Beatrice, Sinilnikova, Olga M, McGuffog, Lesley, Antoniou, Antonis C, Chenevix-Trench, Georgia, Spurdle, Amanda B, Couch, Fergus J

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An Outbreak of Multidrug-Resistant Tuberculosis among Hospitalized Patients with the Acquired Immunodeficiency Syndrome von Edlin, Brian R, Tokars, Jerome I, Grieco, Michael H, Crawford, Jack T, Williams, Julie, Sordillo, Emelia M, Ong, Kenneth R, Kilburn, James O, Dooley, Samuel W, Castro, Kenneth G, Jarvis, William R, Holmberg, Scott D

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Mechanisms of Disease: prediction and prevention of breast cancer-cellular and molecular interactions von Howell, Anthony, Sims, Andrew H, Ong, Kai Ren, Harvie, Michelle N, Evans, D Gareth R, Clarke, Robert B

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Sensorineural deafness, enamel abnormalities and nail abnormalities: a case report of Heimler syndrome in identical twin girls von Ong, K.R., Visram, S., McKaig, S., Brueton, L.A.

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Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2 von Osorio, A, Milne, R L, Alonso, R, Pita, G, Peterlongo, P, Teulé, A, Nathanson, K L, Domchek, S M, Rebbeck, T, Lasa, A, Konstantopoulou, I, Hogervorst, F B, Verhoef, S, van Dooren, M F, Jager, A, Ausems, M G E M, Aalfs, C M, van Asperen, C J, Vreeswijk, M, Waisfisz, Q, Van Roozendaal, C E, Ligtenberg, M J, Easton, D F, Peock, S, Cook, M, Oliver, C T, Frost, D, Curzon, B, Evans, D G, Lalloo, F, Eeles, R, Izatt, L, Davidson, R, Adlard, J, Eccles, D, Ong, K-r, Douglas, F, Downing, S, Brewer, C, Walker, L, Nevanlinna, H, Aittomäki, K, Couch, F J, Fredericksen, Z, Lindor, N M, Godwin, A, Isaacs, C, Caligo, M A, Loman, N, Jernström, H, Barbany-Bustinza, G, Liljegren, A, Ehrencrona, H, Stenmark-Askmalm, M, Feliubadaló, L, Manoukian, S, Peissel, B, Zaffaroni, D, Bonanni, B, Fortuzzi, S, Johannsson, O T, Chenevix-Trench, G, Chen, X-C, Beesley, J, Spurdle, A B, Sinilnikova, O M, Healey, S, McGuffog, L, Antoniou, A C, Brunet, J, Radice, P, Benítez, J

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The future of breast cancer prevention von Howell, A, Sims, A, Harvie, M, Ong, KR, Evans, G, Clarke, R

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Effects of oestrogen on gene expression in the epithelium and stroma of the normal human breast von Sims, AH, Ong, KR, Wilson, CL, Howell, A, Clarke, RB

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Extent of investigation and management of cases of ‘unexplained’ mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus von McVeigh, TP, Monahan, KJ, Christopher, J, West, N, Scott, M, Murray, J, Hanson, H, Armstrong, R, Beggs, A, Berlin, C, Boyde, A, Brady, A, Bulmer, J, Burghel, G, Burn, J, Catherwood, M, Cleaver, R, Coad, B, Conti, H, Cook, J, Cope, W, Corbett, G, Crosbie, E, Davidson, R, DeSouza, B, Donaldson, A, Durkie, M, Eccles, D, Foot, N, Frayling, I, George, A, Gerrard, G, Gibson, S, Green, A, Greville-Heygate, S, Hamilton, S, Hart, R, Hodgson, S, Holliday, D, Hoyle, J, Jewell, R, Kemp, Z, Kiely, L, Kiesel, V, Kohut, K, Kristeleit, R, Kumar, A, Lalloo, F, Latchford, A, Lee, N, Lobo, D, Loughrey, M, MacMahon, S, Martin, R, Martin, S, McVeigh, T, Miedzybrodzka, Z, Minshall, E, Monahan, K, Monje-Garcia, L, Morgan, M, Mugalaasi, H, Musgrave, H, Nastali, E, Norbury, G, Ong, KR, Onyeador, N, Pagan, J, Quigley, K, Ratsma, E, Rea, G, Repana, D, Rosenthal, A, Searle, C, Shaw, A, Side, L, Simon, K, Smith, K, Solomons, J, Varde, A, Wiggins, J, Wren, D, Yarram-Smith, L

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Web presence of an integrated delivery system at year one: lessons learned von Ong, Kenneth R., Kingham, Bernadette, Sotiridy, Kate, Kaufman, David, Polkowski, Michelle, Schofield, John

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The contribution of X-linked coding variation to severe developmental disorders von Martin, HC, Gardner, EJ, Samocha, KE, Kaplanis, J, Akawi, N, Sifrim, A, Eberhardt, RY, Tavares, ALT, Neville, MDC, Niemi, MEK, Gallone, G, McRae, J, Borras, S, Clark, C, Dean, J, Miedzybrodzka, Z, Ross, A, Tennant, S, Dabir, T, Donnelly, D, Humphreys, M, Magee, A, McConnell, V, McKee, S, McNerlan, S, Morrison, PJ, Rea, G, Stewart, F, Cole, T, Cooper, N, Cooper-Charles, L, Cox, H, Islam, L, Jarvis, J, Keelagher, R, Lim, D, McMullan, D, Morton, J, Naik, S, O’Driscoll, M, Ong, KR, Osio, D, Ragge, N, Turton, S, Vogt, J, Williams, D, Bodek, S, Donaldson, A, Hills, A, Low, K, Newbury-Ecob, R, Norman, AM, Roberts, E, Scurr, I, Smithson, S, Tooley, M, Abbs, S, Armstrong, R, Dunn, C, Holden, S, Park, SM, Paterson, J, Raymond, L, Reid, E, Sandford, R, Simonic, I, Tischkowitz, M, Woods, G, Bradley, L, Comerford, J, Green, A, Lynch, S, McQuaid, S, Mullaney, B, Berg, J, Goudie, D, Mavrak, E, McLean, J, McWilliam, C, Reavey, E, Azam, T, Cleary, E, Jackson, A, Lam, W, Lampe, A, Moore, D, Porteous, M, Baple, E, Baptista, J, Brewer, C, Castle, B, Kivuva, E, Owens, M, Rankin, J, Shaw-Smith, C, Turner, C, Turnpenny, P, Tysoe, C, Bradley, T, Davidson, R

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Babesiosis, asplenia, and AIDS von Ong, KennethR, Stavropoulos, Christine, Inada, Yori

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Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes von Whitworth, J, Smith, PS, Martin, J-E, West, H, Luchetti, A, Rodger, F, Clark, G, Carss, K, Stephens, J, Stirrups, K, Penkett, C, Mapeta, R, Ashford, S, Megy, K, Shakeel, H, Ahmed, M, Adlard, J, Barwell, J, Brewer, C, Casey, RT, Armstrong, R, Cole, T, Evans, DG, Fostira, F, Greenhalgh, L, Hanson, H, Henderson, A, Hoffman, J, Izatt, L, Kumar, A, Kwong, A, Lalloo, F, Ong, KR, Paterson, J, Park, S-M, Chen-Shtoyerman, R, Searle, C, Side, L, Skytte, A-B, Snape, K, Woodward, ER, NIHR BioResource Rare Diseases Consortium, Tischkowitz, MD, Maher, ER

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Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes von Whitworth, J, Smith, PS, Martin, J-E, West, H, Luchetti, A, Rodger, F, Clark, G, Carss, K, Stephens, J, Stirrups, K, Penkett, C, Mapeta, R, Ashford, S, Megy, K, Shakeel, H, Ahmed, M, Adlard, J, Barwell, J, Brewer, C, Casey, RT, Armstrong, R, Cole, T, Evans, DG, Fostira, F, Greenhalgh, L, Hanson, H, Henderson, A, Hoffman, J, Izatt, L, Kumar, A, Kwong, A, Lalloo, F, Ong, KR, Paterson, J, Park, S-M, Chen-Shtoyerman, R, Searle, C, Side, L, Skytte, A-B, Snape, K, Woodward, ER, NIHR BioResource Rare Diseases Consortium, Tischkowitz, MD, Maher, ER

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