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    Common Variants at VRK2 and TCF4 Conferring Risk of Schizophrenia von Steinberg, Stacy, de Jong, Simone, Irish Schizophrenia Genomics Consortium, Andreassen, Ole A, Werge, Thomas, Børglum, Anders D, Mors, Ole, Mortensen, Preben B, Gustafsson, Omar, Costas, Javier, Pietiläinen, Olli P.H, Demontis, Ditte, Papiol, Sergi, Huttenlocher, Johanna, Mattheisen, Manuel, Breuer, René, Vassos, Evangelos, Giegling, Ina, Fraser, Gillian, Walker, Nicholas, Tuulio-Henriksson, Annamari, Suvisaari, Jaana, Lönnqvist, Jouko, Paunio, Tiina, Agartz, Ingrid, Melle, Ingrid, Djurovic, Srdjan, Strengman, Eric, GROUP, Jürgens, Gesche, Glenthøj, Birte, Terenius, Lars, Hougaard, David M, Orntoft, Torben, Wiuf, Carsten, Didriksen, Michael, Hollegaard, Mads V, Nordentoft, Merete, van Winkel, Ruud, Kenis, Gunter, Abramova, Lilia, Kaleda, Vasily, Arrojo, Manuel, Sanjuán, Julio, Arango, Celso, Sperling, Swetlana, Rossner, Moritz, Ribolsi, Michele, Magni, Valentina, Siracusano, Alberto, Christiansen, Claus, Kiemeney, Lambertus A, Veldink, Jan, van den Berg, Leonard, Ingason, Andres, Muglia, Pierandrea, Murray, Robin, Nöthen, Markus M, Sigurdsson, Engilbert, Petursson, Hannes, Thorsteinsdottir, Unnur, Kong, Augustine, Rubino, I. Alex, De Hert, Marc, Réthelyi, János M, Bitter, István, Jönsson, Erik G, Golimbet, Vera, Carracedo, Angel, Ehrenreich, Hannelore, Craddock, Nick, Owen, Michael J, O'Donovan, Michael C, Wellcome Trust Case Control Consortium, Ruggeri, Mirella, Tosato, Sarah, Peltonen, Leena, Ophoff, Roel A, Collier, David A, St Clair, David, Rietschel, Marcella, Cichon, Sven, Stefansson, Hreinn, Rujescu, Dan, Stefansson, Kari

    Veröffentlicht in Human Molecular Genetics

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