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Travaglini, Lorena; Brancati, Francesco; Silhavy, Jennifer; Iannicelli, Miriam; Nickerson, Elizabeth; Elkhartoufi, Nadia; Scott, Eric; Spencer, Emily; Gabriel, Stacey; Thomas, Sophie; Ben-Zeev, Bruria; Bertini, Enrico; Boltshauser, Eugen; Chaouch, Malika; Cilio, Maria Roberta; de Jong, Mirjam M; Kayserili, Hulya; Ogur, Gonul; Poretti, Andrea; Signorini, Sabrina; Uziel, Graziella; Zaki, Maha S; Johnson, Colin; AttiƩ-Bitach, Tania; Gleeson, Joseph G; Valente, Enza Maria (2013). Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders. European Journal of Human Genetics, 21(10):1074-1078.

Barbieri, Christopher E; Baca, Sylvan C; Lawrence, Michael S; Demichelis, Francesca; Blattner, Mirjam; Theurillat, Jean-Philippe; White, Thomas A; Stojanov, Petar; Van Allen, Eliezer; Stransky, Nicolas; Nickerson, Elizabeth; Chae, Sung-Suk; Boysen, Gunther; Auclair, Daniel; Onofrio, Robert C; Park, Kyung; Kitabayashi, Naoki; Macdonald, Theresa Y; Sheikh, Karen; Vuong, Terry; Guiducci, Candace; Cibulskis, Kristian; Sivachenko, Andrey; Carter, Scott L; Saksena, Gordon; Voet, Douglas; Hussain, Wasay M; Ramos, Alex H; Winckler, Wendy; Redman, Michelle C; Ardlie, Kristin; Tewari, Ashutosh K; Mosquera, Juan Miguel; Rupp, Niels; Wild, Peter J; Moch, Holger; Morrissey, Colm; Nelson, Peter S; Kantoff, Philip W; Gabriel, Stacey B; Golub, Todd R; Meyerson, Matthew; Lander, Eric S; Getz, Gad; Rubin, Mark A; Garraway, Levi A (2012). Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer. Nature Genetics, 44(6):685-689.

This list was generated on Sat Sep 23 19:13:52 2017 CEST.