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Cell, ISSN 0092-8674, 03/2014, Volume 156, Issue 6, pp. 1324 - 1335
Synonymous mutations change the sequence of a gene without directly altering the sequence of the encoded protein. Here, we present evidence that these “silent”... 
CELL LUNG-CANCER | SILENT MUTATIONS | PROTEIN | TRANSLATION EFFICIENCY | GENE | EXONIC SPLICING ENHANCERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | IDENTIFICATION | VARIANT | SOMATIC MUTATIONS | GENOME | CELL BIOLOGY | Genes, p53 | RNA Splicing | RNA Splice Sites | Neoplasms - genetics | Base Sequence | Humans | Mutation | 3' Untranslated Regions | Oncogenes | RNA | Analysis | Genes | Stem cells | Genetic research | Genetic aspects | Tumor proteins | Cancer
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Journal Article
Ophthalmology, ISSN 0161-6420, 2016, Volume 123, Issue 6, pp. 1375 - 1385
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 10/2011, Volume 365, Issue 15, pp. 1384 - 1395
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Journal Article
by Antoniou, Antonis C and Sinilnikova, Olga M and Simard, Jacques and Léoné, Mélanie and Dumont, Martine and Neuhausen, Susan L and Struewing, Jeffery P and Stoppa-Lyonnet, Dominique and Barjhoux, Laure and Hughes, David J and Coupier, Isabelle and Belotti, Muriel and Lasset, Christine and Bonadona, Valérie and Bignon, Yves-Jean and Rebbeck, Timothy R and Wagner, Theresa and Lynch, Henry T and Domchek, Susan M and Nathanson, Katherine L and Garber, Judy E and Weitzel, Jeffrey and Narod, Steven A and Tomlinson, Gail and Olopade, Olufunmilayo I and Godwin, Andrew and Isaacs, Claudine and Jakubowska, Anna and Lubinski, Jan and Gronwald, Jacek and Górski, Bohdan and Byrski, Tomasz and Huzarski, Tomasz and Peock, Susan and Cook, Margaret and Baynes, Caroline and Murray, Alexandra and Rogers, Mark and Daly, Peter A and Dorkins, Huw and Schmutzler, Rita K and Versmold, Beatrix and Engel, Christoph and Meindl, Alfons and Arnold, Norbert and Niederacher, Dieter and Deissler, Helmut and Spurdle, Amanda B and Chen, Xiaoqing and Waddell, Nicola and Cloonan, Nicole and Kirchhoff, Tomas and Offit, Kenneth and Friedman, Eitan and Kaufmann, Bella and Laitman, Yael and Galore, Gilli and Rennert, Gad and Lejbkowicz, Flavio and Raskin, Leon and Andrulis, Irene L and Ilyushik, Eduard and Ozcelik, Hilmi and Devilee, Peter and Vreeswijk, Maaike P.G and Greene, Mark H and Prindiville, Sheila A and Osorio, Ana and Benítez, Javier and Zikan, Michal and Szabo, Csilla I and Kilpivaara, Outi and Nevanlinna, Heli and Hamann, Ute and Durocher, Francine and Arason, Adalgeir and Couch, Fergus J and Easton, Douglas F and Chenevix-Trench, Georgia and Genetic Modifiers Cancer Risk BRC and GCHBOC and Consortium Invest Modifiers BRCA1 and Epidemiological Study BRCA1 BRCA2 and Kathleen Cuningham Consortium Res and Kathleen Cuningham Consortium for Research into Familial Breast Cancer (kConFab) and German Consortium for Hereditary Breast and Ovarian Cancer (GCHBOC) and Genetic Modifiers of Cancer Risk in BRCA1/2 Mutation Carriers Study (GEMO) and Epidemiological Study of BRCA1 and BRCA2 Mutation Carriers (EMBRACE) and Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
The American Journal of Human Genetics, ISSN 0002-9297, 2007, Volume 81, Issue 6, pp. 1186 - 1200
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