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    Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls von Walsh, R, Lahrouchi, N, Tadros, R, Kyndt, F, Glinge, C, Postema, Pg, Amin, As, Nannenberg, Ea, Ware, Js, Whiffin, N, Mazzarotto, F, Škorić-Milosavljević, D, Krijger, C, Arbelo, E, Babuty, D, Barajas-Martinez, H, Beckmann, Bm, Bézieau, S, Bos, Jm, Breckpot, J, Campuzano, O, Castelletti, S, Celen, C, Clauss, S, Corveleyn, A, Crotti, L, Dagradi, F, de Asmundis, C, Denjoy, I, Dittmann, S, Ellinor, Pt, Ortuño, Cg, Giustetto, C, Gourraud, Jb, Hazeki, D, Horie, M, Ishikawa, T, Itoh, H, Kaneko, Y, Kanters, Jk, Kimoto, H, Kotta, Mc, Krapels, Ipc, Kurabayashi, M, Lazarte, J, Leenhardt, A, Loeys, Bl, Lundin, C, Makiyama, T, Mansourati, J, Martins, Rp, Mazzanti, A, Mörner, S, Napolitano, C, Ohkubo, K, Papadakis, M, Rudic, B, Molina, Ms, Sacher, F, Sahin, H, Sarquella-Brugada, G, Sebastiano, R, Sharma, S, Sheppard, Mn, Shimamoto, K, Shoemaker, Mb, Stallmeyer, B, Steinfurt, J, Tanaka, Y, Tester, Dj, Usuda, K, van der Zwaag, Pa, van Dooren, S, van Laer, L, Winbo, A, Winkel, Bg, Yamagata, K, Zumhagen, S, Volders, Pga, Lubitz, Sa, Antzelevitch, C, Platonov, Pg, Odening, Ke, Roden, Dm, Roberts, Jd, Skinner, Jr, Tfelt-Hansen, J, van den Berg, Mp, Olesen, Ms, Lambiase, Pd, Borggrefe, M, Hayashi, K, Rydberg, A, Nakajima, T, Yoshinaga, M, Saenen, Jb, Kääb, S, Brugada, P, Robyns, T, Giachino, Df

    Veröffentlicht in Genetics in medicine

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    Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls von Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Glinge, Charlotte, Nannenberg, Eline A., Whiffin, Nicola, Mazzarotto, Francesco, Škorić-Milosavljević, Doris, Krijger, Christian, Arbelo, Elena, Breckpot, Jeroen, Campuzano, Oscar, Castelletti, Silvia, Clauss, Sebastian, Crotti, Lia, Dagradi, Federica, de Asmundis, Carlo, Denjoy, Isabelle, Ellinor, Patrick T., Giustetto, Carla, Gourraud, Jean-Baptiste, Hazeki, Daisuke, Horie, Minoru, Ishikawa, Taisuke, Itoh, Hideki, Kaneko, Yoshiaki, Kanters, Jørgen K., Kimoto, Hiroki, Kotta, Maria-Christina, Krapels, Ingrid P.C., Kurabayashi, Masahiko, Loeys, Bart L., Lundin, Catarina, Makiyama, Takeru, Mansourati, Jacques, Mazzanti, Andrea, Mörner, Stellan, Napolitano, Carlo, Ohkubo, Kimie, Papadakis, Michael, Rudic, Boris, Sahin, Hatice, Sarquella-Brugada, Georgia, Sharma, Sanjay, Sheppard, Mary N., Shoemaker, M.Benjamin, Stallmeyer, Birgit, Tanaka, Yuji, Tester, David J., van der Zwaag, Paul A., Van Dooren, Sonia, Van Laer, Lut, Winbo, Annika, Yamagata, Kenichiro, Zumhagen, Sven, Volders, Paul G.A., Lubitz, Steven A., Odening, Katja E., Roden, Dan M., Roberts, Jason D., Skinner, Jonathan R., Tfelt-Hansen, Jacob, van den Berg, Maarten P., Lambiase, Pier D., Borggrefe, Martin, Hayashi, Kenshi, Rydberg, Annika, Nakajima, Tadashi, Yoshinaga, Masao, Saenen, Johan B., Kääb, Stefan, Brugada, Pedro, Robyns, Tomas, Giachino, Daniela F., Brugada, Josep, Gimeno, Juan R., Hasdemir, Can, Guicheney, Pascale, Priori, Silvia G., Schulze-Bahr, Eric, Makita, Naomasa, Schwartz, Peter J., Shimizu, Wataru, Aiba, Takeshi, Schott, Jean-Jacques, Redon, Richard, Ohno, Seiko, Probst, Vincent, Arnaout, Alain Al, Amelot, Mathieu, Anselme, Frédéric, Billon, Olivier, Jesel, Laurence, Laurent, Gabriel, Maury, Philippe, Pasquie, Jean-Luc, Wiart, Francois, Behr, Elijah R., Barc, Julien, Bezzina, Connie R.

    Veröffentlicht in Genetics in medicine

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