Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: SNRPB[original query] |
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Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers. Human molecular genetics 2010 Jul 19 (14): 2886-97. Wang Xianshu, Pankratz V Shane, Fredericksen Zachary, Tarrell Robert, Karaus Mary, McGuffog Lesley, Pharaoh Paul D P, Ponder Bruce A J, Dunning Alison M, Peock Susan, Cook Margaret, Oliver Clare, Frost Debra, , Sinilnikova Olga M, Stoppa-Lyonnet Dominique, Mazoyer Sylvie, Houdayer Claude, , Hogervorst Frans B L, Hooning Maartje J, Ligtenberg Marjolijn J, , Spurdle Amanda, Chenevix-Trench Georgia, , Schmutzler Rita K, Wappenschmidt Barbara, Engel Christoph, Meindl Alfons, Domchek Susan M, Nathanson Katherine L, Rebbeck Timothy R, Singer Christian F, Gschwantler-Kaulich Daphne, Dressler Catherina, Fink Anneliese, Szabo Csilla I, Zikan Michal, Foretova Lenka, Claes Kathleen, Thomas Gilles, Hoover Robert N, Hunter David J, Chanock Stephen J, Easton Douglas F, Antoniou Antonis C, Couch Fergus |
The Core Splicing Factors EFTUD2, SNRPB and TXNL4A Are Essential for Neural Crest and Craniofacial Development. Journal of developmental biology 2022 Jul 10 (3): . Park Byung-Yong, Tachi-Duprat Melanie, Ihewulezi Chibuike, Devotta Arun, Saint-Jeannet Jean-Pier |
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