المؤلفون: Heli Nevanlinna, Carol Anne Gardiner, Alan Donaldson, Philippe Vennin, Michel Longy, Claude Adenis, Gemo, Timothy R. Rebbeck, Karin Kast, Amanda B. Spurdle, Jacques Simard, Allison M. Male, Jean-Pierre Fricker, Antonis C. Antoniou, Dominique Stoppa-Lyonnet, Virginia G. Kaklamani, kConFab, Ursula G. Froster, Rita K. Schmutzler, Fergus J. Couch, Lucy Side, Boris Pasche, Embrace, Ute Hamann, Jean-Philippe Peyrat, Christoph Engel, Beatrix Versmold, Danièle Muller, Irene L. Andrulis, Susan Peock, Dieter Schaefer, J. Fournier, Ian O. Ellis, Mark H. Greene, Csilla Szabo, Georgia Chenevix-Trench, Margaret Cook, Trinidad Caldés Llopis, Anne C. Robinson, Kristiina Aittomäki, Alfons Meindl, Olga M. Sinilnikova, Helen Gregory, Lutecia Pereira, Douglas F. Easton, Patricia Harrington, Louise Emmerson

المصدر: Breast Cancer Research and Treatment. 115:185-192

مصطلحات موضوعية: Adult, Risk, Heterozygote, Cancer Research, Genotype, endocrine system diseases, Genes, BRCA2, Population, Genes, BRCA1, Breast Neoplasms, Biology, Article, Cohort Studies, Breast cancer, Transforming Growth Factor beta, medicine, Humans, Genetic Predisposition to Disease, Allele, Risk factor, skin and connective tissue diseases, education, Alleles, education.field_of_study, Cancer, medicine.disease, Oncology, Mutation, Mutation (genetic algorithm), Cancer research, Female, Breast disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae97654af3d42b4d3c8533dc408cb9a3
https://doi.org/10.1007/s10549-008-0064-8