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    Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants von Kathiresan, Sekar, Voight, Benjamin F, Purcell, Shaun, Musunuru, Kiran, Ardissino, Diego, Mannucci, Pier M, Anand, Sonia, Engert, James C, Samani, Nilesh J, Schunkert, Heribert, Erdmann, Jeanette, Reilly, Muredach P, Rader, Daniel J, Morgan, Thomas, Spertus, John A, Stoll, Monika, Girelli, Domenico, McKeown, Pascal P, Patterson, Chris C, Siscovick, David S, O'Donnell, Christopher J, Elosua, Roberto, Peltonen, Leena, Salomaa, Veikko, Schwartz, Stephen M, Melander, Olle, Altshuler, David, Merlini, Pier Angelica, Berzuini, Carlo, Bernardinelli, Luisa, Peyvandi, Flora, Tubaro, Marco, Celli, Patrizia, Ferrario, Maurizio, Fetiveau, Raffaela, Marziliano, Nicola, Casari, Giorgio, Galli, Michele, Ribichini, Flavio, Rossi, Marco, Bernardi, Francesco, Zonzin, Pietro, Piazza, Alberto, Yee, Jean, Friedlander, Yechiel, Marrugat, Jaume, Lucas, Gavin, Subirana, Isaac, Sala, Joan, Ramos, Rafael, Meigs, James B, Williams, Gordon, Nathan, David M, MacRae, Calum A, Havulinna, Aki S, Berglund, Goran, Hirschhorn, Joel N, Asselta, Rosanna, Duga, Stefano, Spreafico, Marta, Daly, Mark J, Nemesh, James, Korn, Joshua M, McCarroll, Steven A, Surti, Aarti, Guiducci, Candace, Gianniny, Lauren, Mirel, Daniel, Parkin, Melissa, Burtt, Noel, Gabriel, Stacey B, Thompson, John R, Braund, Peter S, Wright, Benjamin J, Balmforth, Anthony J, Ball, Stephen G, Hall, Alistair S

    Veröffentlicht in Nature genetics

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