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, Heikkinen, Tuomas
, Simard, Jacques, Spurdle, Amanda B.
, Beesley, Jonathan
, Chen, Xiaoqing, Neuhausen, Susan L., Ding, Yuan C., Couch, Fergus J., Wang, Xianshu, Fredericksen, Zachary, Peterlongo, Paolo
, Peissel, Bernard
, Bonanni, Bernardo, Viel, Alessandra
, Bernard, Loris, Radice, Paolo
, Szabo, Csilla I., Foretova, Lenka, Zikan, Michal
, Claes, Kathleen
, Greene, Mark H., Mai, Phuong L., Rennert, Gad, Lejbkowicz, Flavio, Andrulis, Irene L., Ozcelik, Hilmi, Glendon, Gord, Gerdes, Anne-Marie
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, Osorio, Ana
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, Lasa, Adriana
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, van der Luijt, Rob B.
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, Kosarin, Kristi
, Offit, Kenneth, Piedmonte, Marion, Rodriguez, Gustavo C., Wakeley, Katie, Boggess, John F., Basil, Jack, Schwartz, Peter E., Blank, Stephanie V., Toland, Amanda E., Montagna, Marco, Casella, Cinzia, Imyanitov, Evgeny N., Allavena, Anna, Schmutzler, Rita K., Versmold, Beatrix, Engel, Christoph, Meindl, Alfons
, Ditsch, Nina, Arnold, Norbert, Niederacher, Dieter
, Deißler, Helmut, Fiebig, Britta, Suttner, Christian, Schönbuchner, Ines, Gadzicki, Dorothea, Caldes, Trinidad, de la Hoya, Miguel, Pooley, Karen A.
, Easton, Douglas F., Chenevix-Trench, Georgia und make_name_string expected hash reference
(2009)
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.
Human Molecular Genetics 18 (22), S. 4442-4456.
Volltext nicht vorhanden.
, Stienen, D, Uhlhaas, S, Stolte, M, Entius, M M, Loff, S, Back, W, Kaufmann, A, Keller, K-M, Blaas, S H, Siebert, R, Vogt, S, Spranger, S, Holinski-Feder, E, Sunde, L
, Propping, P und Friedl, W
(2007)
High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome.
Journal of Medical Genetics 44 (11), S. 702-709.
Volltext nicht vorhanden.
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