المؤلفون: Carolien M. Kets, M. A. Legdeur, Jan C. Oosterwijk, Ellen M. A. Smets, Christianne A.R. Lok, Marian J.E. Mourits, L. E. van der Kolk, M. R. Buist, Cora M. Aalfs, I. van de Beek, J.A. de Hullu

المساهمون: Damage and Repair in Cancer Development and Cancer Treatment (DARE), Targeted Gynaecologic Oncology (TARGON), Human genetics, Human Genetics, Medical Psychology, APH - Personalized Medicine, APH - Quality of Care, Obstetrics and Gynaecology

المصدر: van de Beek, I, Smets, E M A, Legdeur, M A, de Hullu, J A, Lok, C A R, Buist, M R, Mourits, M J E, Kets, C M, van der Kolk, L E, Oosterwijk, J C & Aalfs, C M 2020, ' Genetic counseling of patients with ovarian carcinoma: acceptance, timing, and psychological wellbeing ', Journal of Community Genetics, vol. 11, no. 2, pp. 183-191 . https://doi.org/10.1007/s12687-019-00427-6Test
Journal of Community Genetics
Journal of Community Genetics, 11, 2, pp. 183-191
Journal of community genetics, 11(2), 183-191. SPRINGER HEIDELBERG
Journal of Community Genetics, 11(2), 183-191. Springer Verlag
Journal of Community Genetics, 11, 183-191
Journal of community genetics, 11(2), 183-191. Springer Verlag

مصطلحات موضوعية: medicine.medical_specialty, Genetic testing, endocrine system diseases, Epidemiology, media_common.quotation_subject, Genetic counseling, HOSPITAL ANXIETY, Hospital Anxiety and Depression Scale, BREAST, 03 medical and health sciences, 0302 clinical medicine, DISTRESS, medicine, CANCER PATIENTS, Ovarian carcinoma, Genetics (clinical), media_common, RISK, 0303 health sciences, medicine.diagnostic_test, business.industry, 030305 genetics & heredity, Public Health, Environmental and Occupational Health, Questionnaire, WOMEN, GERMLINE MUTATIONS, DEPRESSION, Women's cancers Radboud Institute for Health Sciences [Radboudumc 17], 3. Good health, Distress, FALLOPIAN-TUBE, 030220 oncology & carcinogenesis, Family medicine, BRCA1/2 MUTATION CARRIERS, Original Article, Worry, Psychological wellbeing, business, Psychosocial

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d41c06cd61f8ef6a8e3458960760585fTest
https://hdl.handle.net/11370/cba29a37-a317-4c15-88ce-435b808fdf42Test

المؤلفون: Mia M Gaudet, Karoline B Kuchenbaecker, Joseph Vijai, Robert J Klein, Tomas Kirchhoff, Lesley McGuffog, Daniel Barrowdale, Alison M Dunning, Andrew Lee, Joe Dennis, Sue Healey, Ed Dicks, Penny Soucy, Olga M Sinilnikova, Vernon S Pankratz, Xianshu Wang, Ronald C Eldridge, Daniel C Tessier, Daniel Vincent, Francois Bacot, Frans B L Hogervorst, Susan Peock, Dominique Stoppa-Lyonnet, KConFab Investigators, Paolo Peterlongo, Rita K Schmutzler, Katherine L Nathanson, Marion Piedmonte, Christian F Singer, Mads Thomassen, Ontario Cancer Genetics Network, Thomas v O Hansen, Susan L Neuhausen, Ignacio Blanco, Mark H Greene, Judith Garber, Jeffrey N Weitzel, Irene L Andrulis, David E Goldgar, Emma D'Andrea, Trinidad Caldes, Heli Nevanlinna, Ana Osorio, Elizabeth J van Rensburg, Adalgeir Arason, Gad Rennert, Ans M W van den Ouweland, Annemarie H van der Hout, Carolien M Kets, Cora M Aalfs, Juul T Wijnen, Margreet G E M Ausems, HEBON, EMBRACE, Debra Frost, Steve Ellis, Elena Fineberg, Radka Platte, D Gareth Evans, Chris Jacobs, Julian Adlard, Marc Tischkowitz, Mary E Porteous, Francesca Damiola, GEMO Study Collaborators, Lisa Golmard, Laure Barjhoux, Michel Longy, Muriel Belotti, Sandra Fert Ferrer, Sylvie Mazoyer, Amanda B Spurdle, Siranoush Manoukian, Monica Barile, Maurizio Genuardi, Norbert Arnold, Alfons Meindl, Christian Sutter, Barbara Wappenschmidt, Susan M Domchek, Georg Pfeiler, Eitan Friedman, Uffe Birk Jensen, Mark Robson, Sohela Shah, Conxi Lazaro, Phuong L Mai, Javier Benitez, Melissa C Southey, Marjanka K Schmidt, Peter A Fasching, Julian Peto, Manjeet K Humphreys, Qin Wang, Kyriaki Michailidou, Elinor J Sawyer, Barbara Burwinkel, Pascal Guénel, Stig E Bojesen, Roger L Milne, Hermann Brenner, Magdalena Lochmann, GENICA Network, Kristiina Aittomäki, Thilo Dörk, Sara Margolin, Arto Mannermaa, Diether Lambrechts, Jenny Chang-Claude, Paolo Radice, Graham G Giles, Christopher A Haiman, Robert Winqvist, Peter Devillee, Montserrat García-Closas, Nils Schoof, Maartje J Hooning, Angela Cox, Paul D P Pharoah, Anna Jakubowska, Nick Orr, Anna González-Neira, Guillermo Pita, M Rosario Alonso, Per Hall, Fergus J Couch, Jacques Simard, David Altshuler, Douglas F Easton, Georgia Chenevix-Trench, Antonis C Antoniou, Kenneth Offit

المصدر: PLoS Genetics, Vol 9, Iss 3, p e1003173 (2013)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23544012/pdf/?tool=EBITest; https://doaj.org/toc/1553-7390Test; https://doaj.org/toc/1553-7404Test

الوصول الحر: https://doaj.org/article/f45b7c806857476fa2644c704c807fc3Test

المؤلفون: T.M. Mooij, Daniel Barrowdale, Christoph Engel, Yen Y. Tan, Christian F. Singer, Shirley Hodgson, Trinidad Caldés, Rosemarie Davidson, Karoline Kuchenbaecker, Sarah Jervis, Wendy K. Chung, D. Gareth Evans, Daniel R. Barnes, Jean-Pierre Fricker, Debra Frost, Dominique Stoppa-Lyonnet, Marc Tischkowitz, Nadine Andrieu, Edith Olah, Lesley McGuffog, Douglas F. Easton, Ana Osorio, Kelly-Anne Phillips, Lenka Foretova, Catherine Noguès, Mary B. Daly, Michael Friedlander, Julian Adlard, Karin Kast, Saundra S. Buys, Steve Ellis, Carolien M. Kets, Maartje J. Hooning, Esther M. John, Eva Machackova, Marie-José Roos-Blom, Muriel A. Adank, Brita Arver, John L. Hopper, Flora E. van Leeuwen, Sue-Anne McLachlan, Pascaline Berthet, Irene L. Andrulis, Kai-ren Ong, Ros Eeles, Antonis C. Antoniou, Louise Izatt, Melissa C. Southey, Mary Beth Terry, Laurence Faivre, David E. Goldgar, Anna Jakubowska, Roger L. Milne, Christine Lasset, Anne-Marie Gerdes, Håkan Olsson, Rita K. Schmutzler, Jacques Simard, Matti A. Rookus, Lizet E. van der Kolk

المساهمون: APH - Quality of Care, APH - Methodology, Other departments

المصدر: Jama : Journal of the American Medical Association, 317, 23, pp. 2402-2416
JAMA, 317(23), 2402-2416. American Medical Association
Jama : Journal of the American Medical Association, 317, 2402-2416
Kuchenbaecker, K B, Hopper, J L, Barnes, D R, Phillips, K-A, Mooij, T M, Roos-Blom, M-J, Jervis, S, McGuffog, L, Evans, D, Barrowdale, D, Frost, D, Adlard, J, Ong, K, Izatt, L, Tischkowitz, M, Eeles, R, Davidson, R, Hodgson, S, Ellis, S, Nogues, C, Lasset, C, Stoppa-Lyonnet, D, Fricker, J-P, Faivre, L, Berthet, P, Hooning, M J, van der Kolk, L, Kets, C M, Adank, M A, John, E M, Chung, W K, Andrulis, I L, Southey, M, Daly, M B, Buys, S S, Osorio, A, Engel, C, Kast, K, Schmutzler, R K, Caldes, T, Jakubowska, A, Simard, J, Friedlander, M L, McLachlan, S A, Machackova, E, Foretova, L, Tan, Y Y, Singer, C F, Olah, E, Gerdes, A-M, Arver, B, Olsson, H, van Leeuwen, F E, Milne, R L, Andrieu, N, Goldgar, D E, Terry, M B, Rookus, M A, Easton, D F & Antoniou, A C 2017, ' Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers ', JAMA: The Journal of the American Medical Association . https://doi.org/10.1001/jama.2017.7112Test

مصطلحات موضوعية: 0301 basic medicine, Oncology, Time Factors, Family Cancer History, endocrine system diseases, Genes, BRCA2, Genes, BRCA1, 0302 clinical medicine, Breast cancer, Interquartile range, Medicine, Prospective Studies, Family history, Prospective cohort study, skin and connective tissue diseases, Aged, 80 and over, Ovarian Neoplasms, education.field_of_study, Obstetrics, Incidence, Age Factors, Neoplasms, Second Primary, General Medicine, Middle Aged, Women's cancers Radboud Institute for Health Sciences [Radboudumc 17], 030220 oncology & carcinogenesis, Female, Adult, medicine.medical_specialty, Population, Breast Neoplasms, Risk Assessment, Cancer predisposition, Familial cancer, 03 medical and health sciences, Age Distribution, Ovarian cancer, Internal medicine, Humans, Family, education, Aged, business.industry, Cancer, medicine.disease, BRCA1, BRCA2, 030104 developmental biology, Mutation, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3f2558bb2dbc69b1a74b204cc16a4c0Test
https://doi.org/10.1001/jama.2017.7112Test

المؤلفون: Caroline Seynaeve, Katja Harbst, Eric A. Ross, Nandita Mitra, Elisa Alducci, Marco Montagna, Janusz Menkiszak, Marion Gauthier-Villars, Javier Benitez, Carole Brewer, Etienne Rouleau, Inge Søkilde Pedersen, Orland Diez, Anya Kushnir, Antonis C. Antoniou, Christine Rappaport, Florentia Fostira, Maurizio Genuardi, Simona Agata, Mark H. Greene, Mary Beth Terry, Nicola Dikow, David E. Goldgar, Anna Jakubowska, Min Hyuk Lee, Sylvie Mazoyer, Diana Eccles, Shirley Hodgson, Anne-Marie Gerdes, Alexander Miron, Laima Tihomirova, Alan Donaldson, Adalgeir Arason, Rosalind A. Eeles, Fergus J. Couch, Hans Jörg Plendl, Francesca Vignolo-Lutati, Ute Hamann, Jackie Cook, Torben A Kruse, Shani Paluch-Shimon, Lisa Walker, Doris Steinemann, Dorothea Gadzicki, Juul T. Wijnen, Markus C. Fleisch, Kenneth Offit, Mary B. Daly, Jamal Zidan, Georgia Chenevix-Trench, Stephanie V. Blank, Marc Tischkowitz, Esther Darder, Annette Fontaine, Louise Izatt, Elżbieta Złowocka-Perłowska, Nadia Boutry-Kryza, Frans B. L. Hogervorst, Stefanie Engert, Danièle Muller, Susan M. Domchek, Phuong L. Mai, Senno Verhoef, Bernhard H. F. Weber, Cecilia M. Dorfling, Kathleen Claes, Kristiina Aittomäki, Annemarie H. van der Hout, Sharon Sand, Olufunmilayo I. Olopade, Margreet G. E. M. Ausems, Aleksandra Tołoczko-Grabarek, Trevor Cole, Giulietta Scuvera, Ana Osorio, Niklas Loman, Timothy R. Rebbeck, Riccardo Dolcetti, Marit Beer, Harsh B. Pathak, Douglas F. Easton, Lone Sunde, Conxi Lázaro, Raanan Berger, Paolo Radice, Mads Thomassen, Ignacio Blanco, Joseph Vijai, Kristie Bobolis, János Papp, Jean-Pierre Fricker, Christine Walsh, Patricia A. Ganz, Marie Stenmark-Askmalm, Andrea Gehrig, Vernon S. Pankratz, Atocha Romero, Xianshu Wang, Loris Bernard, Viviana Gismondi, Mary Porteous, Muy-Kheng Tea, Karen H. Lu, Gustavo C. Rodriguez, Bernardo Bonanni, Christoph Mundhenke, Julian Adlard, Bent Ejlertsen, Dominique Stoppa-Lyonnet, Nadine Tung, Patrick J. Morrison, Dezheng Huo, Cezary Cybulski, Jack Basil, Georg Pfeiler, Daphne Gschwantler-Kaulich, Heli Nevanlinna, Anders Bojesen, Marion Piedmonte, Katherine L. Nathanson, Amanda E. Toland, Sung-Won Kim, Judy Garber, Amanda B. Spurdle, Noralane M. Lindor, Sanne Traasdahl Moeller, Hans Ehrencrona, Trinidad Caldés, Rosemarie Davidson, Karin Kast, Jenny Lester, Shan Wang-Gohrke, Norbert Arnold, Ana Peixoto, Christine Lasset, Andreas Berger, Olga M. Sinilnikova, Katie Wakely, Claude Houdayer, Mercedes Durán, Robert L. Nussbaum, Ramūnas Janavičius, Christina G. Selkirk, Paolo Aretini, Nina Ditsch, J. Margriet Collée, Rosa B. Barkardottir, Sue Healey, Tomasz Huzarski, Cora M. Aalfs, Gillian Mitchell, Peter J. Hulick, Encarna B. Gomez Garcia, Zakaria Einbeigi, Christian F. Singer, Leigha Senter, Yuan Chun Ding, Dieter Niederacher, Yael Laitman, Siranoush Manoukian, Christoph Engel, Anne De Paepe, Anneliese Fink-Retter, Irene L. Andrulis, Rachel Laframboise, Maria A. Caligo, Priyanka Sharma, Miguel de la Hoya, Teresa Ramón y Cajal, Bruce Poppe, Thomas Hansen, Francesca Damiola, Anne-Bine Skytte, Susan L. Neuhausen, Christian Sutter, Marie-Agnès Collonge-Rame, Johannes J. P. Gille, Barbara Pasini, Wendy K. Chung, Noah D. Kauff, M. John Kennedy, Diana Torres, Salina B. Chan, Mark E. Robson, Elizabeth J. van Rensburg, Eric Hahnen, Barbara Wappenschmidt, Grzegorz Sukiennicki, Esther M. John, Rohini Rau-Murthy, Alice S. Whittemore, Kunle Odunsi, Masoud Azodi, John F. Boggess, Sue K. Park, Rita K. Schmutzler, Muriel Belotti, Jeffrey N. Weitzel, Simon A. Gayther, Fei Wan, Andrew K. Godwin, Arjen R. Mensenkamp, Daniela Zaffaroni, Jacques Simard, Susan Peock, Soo Hwang Teo, Claus R. Bartram, Evgeny N. Imyanitov, Maria-Isabel Tejada, Giuseppe Giannini, Mónica Salinas, Banu Arun, Jan C. Oosterwijk, Jacek Gronwald, Alexandra Becker, Tara M. Friebel, Lenka Foretova, Catherine Noguès, Muhammad Usman Rashid, Valeria Pensotti, Antonella Savarese, Debra Frost, Beatrice Melin, Drakoulis Yannoukakos, Steve Ellis, Jean-Philippe Peyrat, Hagay Sobol, Kim De Leeneer, Radka Platte, Jan Lubinski, Javier Godino, Lesley McGuffog, Tomasz Byrski, Claudine Isaacs, Johanna Rantala, Kelly-Anne Phillips, Carolien M. Kets, Uffe Birk Jensen, Katarzyna Durda, Linda Steele, Beth Y. Karlan, Ava Kwong, Alfons Meindl, Lucia Guidugli, Raymonda Varon-Mateeva, D. Gareth Evans, Edith Olah, Isabelle Mortemousque, Manuel R. Teixeira, Joyce Seldon, Katarzyna Jaworska-Bieniek, Bernard Peissel, Saundra S. Buys, Peter Devilee, Kerstin Rhiem, Eitan Friedman

المساهمون: RS: GROW - Oncology, RS: GROW - R4 - Reproductive and Perinatal Medicine, Damage and Repair in Cancer Development and Cancer Treatment (DARE), Targeted Gynaecologic Oncology (TARGON), Cancer Research UK, National Institutes of Health (US), University of Pennsylvania, Breast Cancer Research Foundation, Human Genetics, Human genetics, Epidemiology and Data Science

المصدر: BASE-Bielefeld Academic Search Engine
Rebbeck, T R, Mitra, N, Wan, F, Sinilnikova, O M, Healey, S, McGuffog, L, Mazoyer, S, Chenevix-Trench, G, Easton, D F, Antoniou, A C, Nathanson, K L, Laitman, Y, Kushnir, A, Paluch-Shimon, S, Berger, R, Zidan, J, Friedman, E, Ehrencrona, H, Stenmark-Askmalm, M, Einbeigi, Z, Loman, N, Harbst, K, Rantala, J, Melin, B, Huo, D, Olopade, O I, Seldon, J, Ganz, P A, Nussbaum, R L, Chan, S B, Odunsi, K, Gayther, S A, Domchek, S M, Arun, B K, Lu, K H, Mitchell, G, Karlan, B Y, Walsh, C, Lester, J, Godwin, A K, Pathak, H, Ross, E, Gerdes, A-M, Hansen, T V O, Bojesen, A, Thomassen, M, Moeller, S T, Kruse, T A, Pedersen, I S, Skytte, A-B & CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', J A M A: The Journal of the American Medical Association, vol. 313, no. 13, pp. 1347-1361 . https://doi.org/10.1001/jama.2014.5985Test
JAMA-Journal of the American Medical Association, 313(13), 1347-1361. American Medical Association
JAMA-Journal of the American Medical Association, 313(13), 1347-1361. AMER MEDICAL ASSOC
Digital.CSIC. Repositorio Institucional del CSIC
instname
Jama : Journal of the American Medical Association, 313, 13, pp. 1347-61
JAMA, 313(13), 1347-1361. American Medical Association
Rebbeck, T R, Mitra, N, Wan, F, Sinilnikova, O M, Healey, S, McGuffog, L, Mazoyer, S, Chenevix-Trench, G, Easton, D F, Antoniou, A C, Nathanson, K L, Laitman, Y, Kushnir, A, Paluch-Shimon, S, Berger, R, Zidan, J, Friedman, E, Ehrencrona, H, Stenmark-Askmalm, M, Einbeigi, Z, Loman, N, Harbst, K, Rantala, J, Melin, B, Huo, D, Olopade, O I, Seldon, J, Ganz, P A, Nussbaum, R L, Chan, S B, Odunsi, K, Gayther, S A, Domchek, S M, Arun, B K, Lu, K H, Mitchell, G, Karlan, B Y, Walsh, C, Lester, J, Godwin, A K, Pathak, H, Ross, E, Daly, M B, Whittemore, A S, John, E M, Miron, A, Terry, M B, Chung, W K, Goldgar, D E, Pedersen, I S & CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', JAMA: The Journal of the American Medical Association, vol. 313, no. 13, pp. 1347-61 . https://doi.org/10.1001/jama.2014.5985Test
CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', JAMA, vol. 313, no. 13, pp. 1347-61 . https://doi.org/10.1001/jama.2014.5985Test
Jama : Journal of the American Medical Association, 313, 1347-61
Rebbeck, T R, Mitra, N, Wan, F, Sinilnikova, O M, Healey, S, McGuffog, L, Mazoyer, S, Chenevix-Trench, G, Easton, D F, Antoniou, A C, Nathanson, K L, Laitman, Y, Kushnir, A, Paluch-Shimon, S, Berger, R, Zidan, J, Friedman, E, Ehrencrona, H, Stenmark-Askmalm, M, Einbeigi, Z, Loman, N, Harbst, K, Rantala, J, Melin, B, Huo, D, Olopade, O I, Seldon, J, Ganz, P A, Nussbaum, R L, Chan, S B, Odunsi, K, Gayther, S A, Domchek, S M, Arun, B K, Lu, K H, Mitchell, G, Karlan, B Y, Walsh, C, Lester, J, Godwin, A K, Pathak, H, Ross, E, Daly, M B, Whittemore, A S, John, E M, Miron, A, Pedersen, I S, Skytte, A-B, Sunde, L, Jensen, U B & CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', JAMA: The Journal of the American Medical Association, vol. 313, no. 13, pp. 1347-61 . https://doi.org/10.1001/jama.2014.5985Test
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
JAMA, 313(13), 1347-61. American Medical Association

مصطلحات موضوعية: endocrine system diseases, Genes, BRCA2, MathematicsofComputing_GENERAL, Genes, BRCA1, cancer risk, Settore MED/03 - GENETICA MEDICA, medicine.disease_cause, MOUSE MODELS, Risk Factors, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Age of Onset, POSITION, skin and connective tissue diseases, Adult, Breast Neoplasms, Female, Heterozygote, Humans, Middle Aged, Nucleotides, Ovarian Neoplasms, Genetic Predisposition to Disease, Mutation, Medicine (all), MESSENGER-RNA DECAY, UNKNOWN CLINICAL-SIGNIFICANCE, BRCA1 and BRCA2 genes, mutation type and position, cancer risk, TheoryofComputation_GENERAL, General Medicine, GERMLINE MUTATIONS, CARRIERS, 3. Good health, SUSCEPTIBILITY GENE, Medical genetics, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9], medicine.medical_specialty, PROTEINS, mutation type and position, BRCA1 and BRCA2 genes, DNA-SEQUENCE VARIANTS, Article, REGION, Breast cancer, Germline mutation, medicine, BRCA1 or BRCA2, business.industry, Cancer, Heterozygote advantage, medicine.disease, Cancer research, Age of onset, Ovarian cancer, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0415ece5c738d9598312bc28311732caTest
https://doi.org/10.1001/jama.2014.5985Test

المؤلفون: Karoline B. Kuchenbaecker, Lesley McGuffog, Daniel Barrowdale, Andrew Lee, Penny Soucy, Sue Healey, Joe Dennis, Michael Lush, Mark Robson, Amanda B. Spurdle, Susan J. Ramus, Nasim Mavaddat, Mary Beth Terry, Susan L. Neuhausen, Ute Hamann, Melissa Southey, Esther M. John, Wendy K. Chung, Mary B. Daly, Saundra S. Buys, David E. Goldgar, Cecilia M. Dorfling, Elizabeth J. van Rensburg, Yuan Chun Ding, Bent Ejlertsen, Anne-Marie Gerdes, Thomas V. O. Hansen, Susan Slager, Emily Hallberg, Javier Benitez, Ana Osorio, Nancy Cohen, William Lawler, Jeffrey N. Weitzel, Paolo Peterlongo, Valeria Pensotti, Riccardo Dolcetti, Monica Barile, Bernardo Bonanni, Jacopo Azzollini, Siranoush Manoukian, Bernard Peissel, Paolo Radice, Antonella Savarese, Laura Papi, Giuseppe Giannini, Florentia Fostira, Irene Konstantopoulou, Julian Adlard, Carole Brewer, Jackie Cook, Rosemarie Davidson, Diana Eccles, Ros Eeles, Steve Ellis, EMBRACE, Debra Frost, Shirley Hodgson, Louise Izatt, Fiona Lalloo, Kai-ren Ong, Andrew K. Godwin, Norbert Arnold, Bernd Dworniczak, Christoph Engel, Andrea Gehrig, Eric Hahnen, Jan Hauke, Karin Kast, Alfons Meindl, Dieter Niederacher, Rita Katharina Schmutzler, Raymonda Varon-Mateeva, Shan Wang-Gohrke, Barbara Wappenschmidt, Laure Barjhoux, Marie-Agne`s Collonge-Rame, Camille Elan, GEMO Study Collaborators, Lisa Golmard, Emmanuelle Barouk-Simonet, Fabienne Lesueur, Sylvie Mazoyer, Joanna Sokolowska, Dominique Stoppa- Lyonnet, Claudine Isaacs, Kathleen B. M. Claes, Bruce Poppe, Miguel de la Hoya, Vanesa Garcia-Barberan, Kristiina Aittom€aki, Heli Nevanlinna, Margreet G. E. M. Ausems, J. L. de Lange, Encarna B. Gomez Garcia, HEBON, Frans B. L. Hogervorst, Carolien M. Kets, Hanne E. J. Meijers-Heijboer, Jan C. Oosterwijk, Matti A. Rookus, Christi J. van Asperen, Ans M. W. van den Ouweland, Helena C. van Doorn, Theo A. M. van Os, Ava Kwong, Edith Olah, Orland Diez, Joan Brunet, Conxi Lazaro, Alex Teule ́, Jacek Gronwald, Anna Jakubowska, Katarzyna Kaczmarek, Jan Lubinski, Grzegorz Sukiennicki, Rosa B. Barkardottir, Jocelyne Chiquette, Simona Agata, Marco Montagna, Manuel R. Teixeira, KConFab Investigators, Sue Kyung Park, Curtis Olswold, Marc Tischkowitz, Lenka Foretova, Pragna Gaddam, Joseph Vijai, Georg Pfeiler, Christine Rappaport-Fuerhauser, Christian F. Singer, Muy-Kheng M. Tea, Mark H. Greene, Jennifer T. Loud, Gad Rennert, Evgeny N. Imyanitov, Peter J. Hulick, John L. Hays, Marion Piedmonte, Gustavo C. Rodriguez, Julie Martyn, Gord Glendon, Anna Marie Mulligan, Irene L. Andrulis, Amanda Ewart Toland, Uffe Birk Jensen, Torben A. Kruse, Inge Sokilde Pedersen, Mads Thomassen, Maria A. Caligo, Soo-Hwang Teo, Raanan Berger, Eitan Friedman, Yael Laitman, Brita Arver, Ake Borg, Hans Ehrencrona, Johanna Rantala, Olufunmilayo I. Olopade, Patricia A. Ganz, Robert L. Nussbaum, Angela R. Bradbury, Susan M. Domchek, Katherine L. Nathanson, Banu K. Arun, Paul James, Beth Y. Karlan, Jenny Lester, Jacques Simard, Paul D. P. Pharoah, Kenneth Offit, Fergus J. Couch, Georgia Chenevix-Trench, Douglas F. Easton, Antonis C. Antoniou

المساهمون: Kuchenbaecker, Karoline B., Mcguffog, Lesley, Barrowdale, Daniel, Lee, Andrew, Soucy, Penny, Healey, Sue, Dennis, Joe, Lush, Michael, Robson, Mark, Spurdle, Amanda B., Ramus, Susan J., Mavaddat, Nasim, Beth Terry, Mary, Neuhausen, Susan L., Hamann, Ute, Southey, Melissa, John, Esther M., Chung, Wendy K., Daly, Mary B., Buys, Saundra S., Goldgar, David E., Dorfling, Cecilia M., van Rensburg, Elizabeth J., Chun Ding, Yuan, Ejlertsen, Bent, Gerdes, Anne-Marie, Hansen, Thomas V. O., Slager, Susan, Hallberg, Emily, Benitez, Javier, Osorio, Ana, Cohen, Nancy, Lawler, William, Weitzel, Jeffrey N., Peterlongo, Paolo, Pensotti, Valeria, Dolcetti, Riccardo, Barile, Monica, Bonanni, Bernardo, Azzollini, Jacopo, Manoukian, Siranoush, Peissel, Bernard, Radice, Paolo, Savarese, Antonella, Papi, Laura, Giannini, Giuseppe, Fostira, Florentia, Konstantopoulou, Irene, Adlard, Julian, Brewer, Carole, Cook, Jackie, Davidson, Rosemarie, Eccles, Diana, Eeles, Ro, Ellis, Steve, Embrace, Frost, Debra, Hodgson, Shirley, Izatt, Louise, Lalloo, Fiona, Ong, Kai-ren, Godwin, Andrew K., Arnold, Norbert, Dworniczak, Bernd, Engel, Christoph, Gehrig, Andrea, Hahnen, Eric, Hauke, Jan, Kast, Karin, Meindl, Alfon, Niederacher, Dieter, Katharina Schmutzler, Rita, Varon-Mateeva, Raymonda, Wang-Gohrke, Shan, Wappenschmidt, Barbara, Barjhoux, Laure, Collonge-Rame, Marie-Agne`, Elan, Camille, Study Collaborators, Gemo, Golmard, Lisa, Barouk-Simonet, Emmanuelle, Lesueur, Fabienne, Mazoyer, Sylvie, Sokolowska, Joanna, Stoppa- Lyonnet, Dominique, Isaacs, Claudine, Claes, Kathleen B. M., Poppe, Bruce, de la Hoya, Miguel, Garcia-Barberan, Vanesa, Aittom€aki, Kristiina, Nevanlinna, Heli, Ausems, Margreet G. E. M., de Lange, J. L., Gomez Garcia, Encarna B., Hebon, Hogervorst, Frans B. L., Kets, Carolien M., Meijers-Heijboer, Hanne E. J., Oosterwijk, Jan C.

مصطلحات موضوعية: Adolescent, Adult, Breast Neoplasm, Female, Genetic Predisposition to Disease, Heterozygote, Human, Middle Aged, Multifactorial Inheritance, Ovarian Neoplasm, Polymorphism, Single Nucleotide, Prognosi, Proportional Hazards Model, Receptors, Estrogen, Risk Assessment, Risk Factor, Young Adult, Genes, BRCA1, BRCA2, Mutation, Oncology, Cancer Research

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28376175; info:eu-repo/semantics/altIdentifier/wos/WOS:000405496200004; volume:109; issue:7; firstpage:2240; lastpage:2250; numberofpages:11; journal:JOURNAL OF THE NATIONAL CANCER INSTITUTE; http://hdl.handle.net/11573/1027716Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85016213460; http://jnci.oxfordjournals.orgTest/

الإتاحة: https://doi.org/10.1093/jnci/djw302Test
http://hdl.handle.net/11573/1027716Test
http://jnci.oxfordjournals.orgTest/

المؤلفون: Marco Montagna, Bruno Buecher, Goska Leslie, Daniel Barrowdale, Anita Bane, Louise Izatt, Eitan Friedman, Yosr Hamdi, Kenneth Offit, Klaartje van Engelen, Soo Hwang Teo, Frans B. L. Hogervorst, Conxi Lázaro, Sylvie Mazoyer, Diana Eccles, Yuan Chun Ding, Laura Papi, Georgia Chenevix-Trench, Katarzyna Kaczmarek, Laima Tihomirova, Jacek Gronwald, Jocelyne Chiquette, Patricia A. Ganz, Thomas P. Slavin, Kathleen Claes, Paolo Radice, Elizabeth J. van Rensburg, Adalgeir Arason, Lenka Foretova, Milena Mariani, Johanna Rantala, Pascaline Berthet, Evgeny N. Imyanitov, Claudine Isaacs, Esther M. John, Maite Laurent, Irene L. Andrulis, Juul T. Wijnen, Paolo Peterlongo, Susan M. Domchek, Banu Arun, Amanda E. Toland, Anna Marie Mulligan, Penny Soucy, Kristiina Aittomäki, Orland Diez, Heli Nevanlinna, Anne-Marie Gerdes, Austin Miller, Olufunmilayo I. Olopade, Raymonda Varon-Mateeva, Alfons Meindl, Cecilia M. Dorfling, Niklas Loman, Paul A. James, Susan L. Neuhausen, Muy Kheng Tea, Inge Søkilde Pedersen, Arnaud Droit, D. Gareth Evans, Mark E. Robson, Jennifer T. Loud, Jan C. Oosterwijk, Judy Garber, Douglas F. Easton, Jacques Simard, Mark H. Greene, Pamela S. Ganschow, Edith Olah, Audrey Lemaçon, Norbert Arnold, Catherine M. Phelan, Gad Rennert, Judy Kirk, Johanna Sokolowska, Tomi Pastinen, Robert L. Nussbaum, Simon A. Gayther, Karoline B. Kuchenbaeker, Mads Thomassen, Ros Eeles, Riccardo Dolcetti, Hanne Meijers-Heijboer, Marc Tischkowitz, George Fountzilas, Laure Barjhoux, Kristie Bobolis, Christoph Engel, Bernardo Bonanni, Sue K. Park, Beth Y. Karlan, Nicolas Sevenet, Bent Ejlertsen, Wendy K. Chung, Timothy R. Rebbeck, Amanda B. Spurdle, Peter J. Hulick, Mary B. Daly, Yen Y. Tan, Annelie Liljegren, Carolien M. Kets, Miguel de la Hoya, Gord Glendon, Mieke Kriege, Rita K. Schmutzler, Manuel R. Teixeira, Christine Rappaport-Fuerhauser, Pedro Pérez Segura, William D. Foulkes, Rosemarie Davidson, Steven N. Hart, Javier Benitez, Jenny Lester, Melissa C. Southey, Ramunas Janavicius, Uffe Birk Jensen, Zakaria Einbeigi, Christian F. Singer, Jacopo Azzollini, Alex Teulé, David E. Goldgar, Ans M.W. van den Ouweland, Anna Jakubowska, Angela R. Bradbury, Dominique Stoppa-Lyonnet, Carole Brewer, Zsofia K. Stadler, Nadine Tung, Eric Hahnen, Vijai Joseph, Grzegorz Sukiennicki, Siranoush Manoukian, Debra Frost, Maria A. Caligo, Andrew K. Godwin, Christian Sutter, Bernard Peissel, Andrea L. Richardson, Kim De Leeneer, Antonis C. Antoniou, Florentia Fostira, Lesley McGuffog, Matti A. Rookus, Mary Beth Terry, Saundra S. Buys, Fabienne Lesueur, Gustavo C. Rodriguez, Julian Adlard, Barbara Wappenschmidt, Marinus J. Blok, Yael Laitman, Rob B. van der Luijt, Thomas Hansen, Francesca Damiola, Katherine L. Nathanson, Silje Nord, Kai Ren Ong, Ana Osorio, Katie Snape, Fergus J. Couch, John L. Hays, Walter Just, Ute Hamann, Silvia Tognazzo, Payal D. Shah, Valérie Bonadona, Ida Marie Heeholm Sonderstrup, Lídia Feliubadaló

المساهمون: RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Lab Centraal Lab (9), European Research Council, Cancer Research UK (Reino Unido), Post-cancer GWAS Initiative, United States Department of Defense, Research Council of Lithuania, Asociación Española Contra el Cáncer, Red Temática de Investigación Cooperativa en Cáncer (España), Fondation ARC pour la recherche sur le cancer, Canadian Institutes of Health Research, Ministère de Économie, Innovation et Exportation (Canadá), University of Kansas. Cancer Center (Estados Unidos), Deutsche Krebshilfe, Leipzig Research Centre for Civilization Diseases, Non-therapeutic Subject Registry Shared Resource at Georgetown University (NIH/NCI), Instituto de Salud Carlos III, Finlands Akademi (Finlandia), Dutch Cancer Society (Holanda), Dutch Research Council (Holanda), Pink Ribbons Project, Biobanking and BioMolecular resources Research Infrastructure (Países Bajos), Transcan Grant JTC Cancer, Hungarian Research Grants, Government of Catalonia (España), Ministry of Health and Welfare (Corea del Sur), United States of Department of Health & Human Services, State Budget of the Czech Republic (RECAMO), Charles University (República Checa), Westat (Estados Unidos), Russian Foundation for Basic Research, GOG Foundation. Gynecologic Oncology Group, Italian Association for Cancer Research, Clinical Genetics, CCA - Cancer biology and immunology, Human genetics, Epidemiology and Data Science, Human Genetics, Leslie, Goska [0000-0001-5756-6222], Tischkowitz, Marc [0000-0002-7880-0628], Easton, Douglas [0000-0003-2444-3247], Antoniou, Antonis [0000-0001-9223-3116], Apollo - University of Cambridge Repository, Medicum, Clinicum, Department of Medical and Clinical Genetics, HUS Gynecology and Obstetrics, Department of Obstetrics and Gynecology, Damage and Repair in Cancer Development and Cancer Treatment (DARE), Targeted Gynaecologic Oncology (TARGON)

المصدر: Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Breast Cancer Research and Treatment, 161(1), 117-134. Springer, Cham
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, De la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadalo, L, Foretova, L, Fostira, F, Pedersen, I S & EMBRACE 2017, ' 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 risk at locus 11q22.3 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2Test
Breast Cancer Research and Treatment, 161(1), 117-134. Springer New York
Breast Cancer Research and Treatment, 161, 1, pp. 117-134
Breast Cancer Research and Treatment, 161, 117-134
Hamdi, Y; Soucy, P; Kuchenbaeker, KB; Pastinen, T; Droit, A; Lemacon, A; et al.(2017). 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 risk at locus 11q22.3. BREAST CANCER RESEARCH AND TREATMENT, 161(1), 117-134. doi: 10.1007/s10549-016-4018-2. UCLA: Retrieved from: http://www.escholarship.org/uc/item/03k1w9cmTest
Breast Cancer Research and Treatment, 161(1), 117-134
Breast Cancer Research and Treatment, 161(1), 117. Springer New York
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, De la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadalo, L, Foretova, L, Jensen, U B, Pedersen, I S & EMBRACE 2017, ' 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 risk at locus 11q22.3 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117–134 . https://doi.org/10.1007/s10549-016-4018-2Test
Breast cancer research and treatment, 161(1), 117-134. Springer New York
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Azzollini, J, Arun, B K, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K A, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, de la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, EMBRACE, Engel, C, Gareth Evans, D, Feliubadaló, L, Foretova, L, Fostira, F, Gerdes, A-M, Easton, D F, Antoniou, A C & Simard, J 2017, ' 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 risk at locus 11q22.3 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2Test
kConFab Investigators, HEBON, GEMO Study Collaborators & EMBRACE 2017, ' 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 risk at locus 11q22.3 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2Test
BREAST CANCER RESEARCH AND TREATMENT
Repisalud
Instituto de Salud Carlos III (ISCIII)
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, De la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadalo, L, Meijers-Heijboer, H E J, Oosterwijk, J C, van Engelen, K, EMBRACE, GEMO Study Collaborators, HEBON & KConFab Investigators 2017, ' 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 risk at locus 11q22.3 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2Test
Breast Cancer Research and Treatment
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benítez, J, Berthet, P, Blok, M J, Bobolis, K A, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, de la Hoya, M, De Leeneer, K, Díez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadaló, L, Foretova, L, Gerdes, A-M, Thomassen, M & EMBRACE 2017, ' 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 risk at locus 11q22.3 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2Test
Breast Cancer Research and Treatment, 161(1), 117-134. SPRINGER

مصطلحات موضوعية: 0301 basic medicine, Genetic modifiers, Cancer Research, Epidemiology, Genes, BRCA2, BRCA1 and BRCA2 mutation carriers, Genes, BRCA1, Gene Expression, Gene mutation, DISEASE, Breast cancer, 3123 Gynaecology and paediatrics, Medicine and Health Sciences, INVESTIGATORS, mutation carriers, skin and connective tissue diseases, Genetics, 1184 Genetics, developmental biology, physiology, 3. Good health, Women's cancers Radboud Institute for Health Sciences [Radboudumc 17], Oncology, Female, Differential allelic expression, Risk, Heterozygote, 3122 Cancers, Quantitative Trait Loci, NPAT, Single-nucleotide polymorphism, Locus (genetics), Breast Neoplasms, Quantitative trait locus, Biology, OVARIAN-CANCER, 03 medical and health sciences, CYCLIN E-CDK2, SDG 3 - Good Health and Well-being, Journal Article, medicine, Genetic predisposition, Genetic susceptibility, Biomarkers, Tumor, Humans, Genetic Predisposition to Disease, Allele, BRCA1 and BRCA2, Alleles, Genetic association, HUMAN-CELLS, Chromosomes, Human, Pair 11, CONSORTIUM, Genetic Variation, DNA, medicine.disease, 030104 developmental biology, Mutation, Cis-regulatory variants, 3111 Biomedicine

وصف الملف: application/pdf; image/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba8cf2d9bb045cb1dbafc6fe95cfcd7bTest
https://hdl.handle.net/20.500.12530/33541Test

المؤلفون: C.J. van Asperen, G. H. de Bock, Carolien M. Kets

المصدر: Bijblijven. 29:29-34

مصطلحات موضوعية: media_common.quotation_subject, General Medicine, Art, Theology, media_common

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::3359b1a1b27e37f77e22af0490a190e3Test
https://doi.org/10.1007/s12414-013-0032-zTest

المؤلفون: Wendy A. G. van Zelst-Stams, Nicoline Hoogerbrugge, Simone Salemink, Erica van der Looij, Nicky Dekker, Carolien M. Kets

المصدر: Journal of Genetic Counseling
Journal of Genetic Counseling, 22, 118-24
Journal of Genetic Counseling, 22, 1, pp. 118-24

مصطلحات موضوعية: Gerontology, Adult, Male, medicine.medical_specialty, Colorectal cancer, Genetic counseling, Hereditary cancer and cancer-related syndromes Genetics and epigenetic pathways of disease [ONCOL 1], Genetic Counseling, Colorectal neoplasms, Young Adult, Surveys and Questionnaires, medicine, Humans, Genetics(clinical), Genetic Predisposition to Disease, Young adult, Family history, Genetics (clinical), Original Research, Aged, Response rate (survey), Health Services Needs and Demand, Hereditary cancer and cancer-related syndromes [ONCOL 1], business.industry, Public health, Cancer, Patient preferences, Middle Aged, medicine.disease, Human genetics, Family medicine, Female, business, Quality of hospital and integrated care [NCEBP 4]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b8619e0ce6df5746ec7cc7c0fa1ac79Test
https://hdl.handle.net/2066/118440Test

المؤلفون: Carolien M. Kets, C.J. van Asperen

المصدر: Bijblijven. 27:14-19

مصطلحات موضوعية: media_common.quotation_subject, General Medicine, Art, Humanities, media_common

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::84d9369fbd7886bfa229b05cd104b756Test
https://doi.org/10.1007/s12414-011-0074-zTest

المؤلفون: George M. Martin, Norberto López, Kivanc Cefle, Davor Lessel, Sukru Ozturk, Junko Oshima, Joerg Schmidtke, P. F. Ippel, Bhaskar Saha, Gudrun Nürnberg, Joseph Boak, Fuki M. Hisama, Dru F. Leistritz, Daniel Eyman, Martin Poot, Katrin Friedrich, Holger Hoehn, Dincy Peter, María J. Garcia-F-Villalta, Lin Lee, Theda Wessel, Carolien M. Kets, Peter Nürnberg, Peter C. van den Akker, Christian Kubisch, Vítor Tedim Cruz, Birgit Groff-Kellermann, Chumei Li, Goli Compoginis

المساهمون: Translational Immunology Groningen (TRIGR)

المصدر: Human Genetics, 128, 103-11
HUMAN GENETICS, 128(1), 103-111. SPRINGER
Human Genetics, 128, 1, pp. 103-11

مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Werner Syndrome Helicase, Mutation, Missense, Locus (genetics), VARIANTS, SYNDROME GENE, Article, Genomic disorders and inherited multi-system disorders [IGMD 3], Chromosome Breakpoints, Exon, NEUREGULIN-1, SCHIZOPHRENIA, Genetics, medicine, Humans, EPIDEMIOLOGY, Missense mutation, SYNDROME LOCUS, education, Genetics (clinical), Werner syndrome, education.field_of_study, RecQ Helicases, IDENTIFICATION, biology, NUCLEAR-LOCALIZATION, DNA HELICASE, nutritional and metabolic diseases, Helicase, medicine.disease, Founder Effect, Introns, SYNDROME PROTEIN, Human genetics, Exodeoxyribonucleases, Mutation, biology.protein, Female, Werner Syndrome, Founder effect

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13b70c3168e5331a43b20253ab0c5c8fTest
https://doi.org/10.1007/s00439-010-0832-5Test