13058_2016_768_MOESM1_ESM.doc (177.5 kB)
Additional file 1: Table S1. of Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women
journal contribution
posted on 2016-11-11, 05:00 authored by Timothy Rebbeck, Tara Friebel, Nandita Mitra, Fei Wan, Stephanie Chen, Irene Andrulis, Paraskevi Apostolou, Norbert Arnold, Banu Arun, Daniel Barrowdale, Javier Benitez, Raanan Berger, Pascaline Berthet, Ake Borg, Saundra Buys, Trinidad Caldes, Jonathan Carter, Jocelyne Chiquette, Kathleen Claes, Fergus Couch, Cezary Cybulski, Mary Daly, Miguel de la Hoya, Orland Diez, Susan Domchek, Katherine Nathanson, Katarzyna Durda, Steve Ellis, D. Evans, Lenka Foretova, Eitan Friedman, Debra Frost, Patricia Ganz, Judy Garber, Gord Glendon, Andrew Godwin, Mark Greene, Jacek Gronwald, Eric Hahnen, Emily Hallberg, Ute Hamann, Thomas Hansen, Evgeny Imyanitov, Claudine Isaacs, Anna Jakubowska, Ramunas Janavicius, Katarzyna Jaworska-Bieniek, Esther John, Beth Karlan, Bella Kaufman, KConFab investigators, Ava Kwong, Yael Laitman, Christine Lasset, Conxi Lazaro, Jenny Lester, Niklas Loman, Jan Lubinski, Siranoush Manoukian, Gillian Mitchell, Marco Montagna, Susan Neuhausen, Heli Nevanlinna, Dieter Niederacher, Robert Nussbaum, Kenneth Offit, Edith Olah, Olufunmilayo Olopade, Sue Park, Marion Piedmonte, Paolo Radice, Christine Rappaport-Fuerhauser, Matti Rookus, Caroline Seynaeve, Jacques Simard, Christian Singer, Penny Soucy, Melissa Southey, Dominique Stoppa-Lyonnet, Grzegorz Sukiennicki, Csilla Szabo, Mariella Tancredi, Manuel Teixeira, Soo-Hwang Teo, Mary Terry, Mads Thomassen, Laima Tihomirova, Marc Tischkowitz, Amanda Toland, Aleksandra Toloczko-Grabarek, Nadine Tung, Elizabeth van Rensburg, Danylo Villano, Shan Wang-Gohrke, Barbara Wappenschmidt, Jeffrey Weitzel, Jamal Zidan, Kristin Zorn, Lesley McGuffog, Douglas Easton, Georgia Chenevix-Trench, Antonis Antoniou, Susan RamusEthics committees that granted approval for the access and use of the data for this study. Table S2. Participant counts by center and mutation. Table S3. Primers used for PCR and Sanger sequencing. Table S4. Primers used in micro-satellite analysis for loss of heterozygosity. Table S5. Micro-satellite loss of heterozygosity and sequencing analysis results. (DOC 177 kb)
