Treffer 1 - 20 von 694 für Suche 'PANGILINAN, A', Suchdauer: 1,80s Treffer weiter einschränken
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    Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations von Smith, Alexander W., Carpay, Johannes A., Devinsky, Orrin, Braun, Kees P. J., Smit, Dirk J. A., Avbersek, Andreja, Becker, Albert J., Berkovic, Samuel F., Boysen, Katja E., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Chinthapalli, Krishna, Coffey, Alison J., Coppola, Antonietta, Cossette, Patrick, De Jonghe, Peter, Dlugos, Dennis J., Feucht, Martha, Freytag, Saskia, Geller, Eric B., Guo, Youling, Hakonarson, Hakon, Haut, Sheryl, Heinzen, Erin L., Hengsbach, Christian, Johnson, Michael R., Kälviäinen, Reetta, Kirsch, Heidi E., Lau, Yu‐Lung, Lehesjoki, Anna‐Elina, Lerche, Holger, Lieb, Wolfgang, Malovini, Alberto, McCormack, Mark, Molloy, Anne M., Rau, Sarah, Schachter, Steven C., Vari, Maria S., Weber, Yvonne G., Weisenberg, Judith, Wolff, Markus, Yang, Wanling, Zara, Federico, Howrigan, Daniel P., Cerrato, Felecia, Gabriel, Stacey B., Daly, Mark J., Neale, Benjamin M., Lowenstein, Daniel H., Cossette, Patrick, Cotsapas, Chris, Petrovski, Slavé, Sisodiya, Sanjay M., Freyer, Catharine, McKenna, Kevin, Bennett, Caitlin A., Burgess, Rosemary, O'Brien, Terence J., Stamberger, Hannah, Krestel, Heinz, Gallati, Sabina, Papacostas, Savvas S., Tanteles, George A., Klein, Karl Martin, Rademacher, Michael, Afawi, Zaid, Korczyn, Amos D., Kanaan, Moien, Lemke, Johannes R., Wolking, Stefan, Schulze‐Bonhage, Andreas, Schubert‐Bast, Susanne, Korinthenberg, Rudolf, Dennig, Dieter, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Rees, Mark I., Schneider, Natascha, Sills, Graeme J., Shukralla, Arif, McCormack, Mark, Canafoglia, Laura, Franceschetti, Silvana, Iacomino, Michele, Stella Vari, Maria, Salpietro, Vincenzo, Labate, Angelo, Manna, Lorella, Parrini, Elena, Inoue, Yushi, Topaloglu, Pınar, Yücesan, Emrah, Poduri, Annapurna, Buono, Russell J., Sperling, Michael R., Lo, Warren, Hegde, Manu, Helbig, Katherine L.

    Veröffentlicht in Epilepsia (Copenhagen)

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    Exome sequencing identifies variants in infants with sacral agenesis von Pitsava, Georgia, Feldkamp, Marcia L., Pankratz, Nathan, Lane, John, Kay, Denise M., Conway, Kristin M., Hobbs, Charlotte, Shaw, Gary M., Reefhuis, Jennita, Jenkins, Mary M., Almli, Lynn M., Moore, Cynthia, Werler, Martha, Browne, Marilyn L., Cunniff, Chris, Olshan, Andrew F., Pangilinan, Faith, Brody, Lawrence C., Sicko, Robert J., Finnell, Richard H., Bamshad, Michael J., McGoldrick, Daniel, Nickerson, Deborah A., Mullikin, James C., Romitti, Paul A., Mills, James L., Brody, Lawrence C., Browne, Marilyn L., Feldkamp, Marcia L., Hobbs, Charlotte, Jenkins, Mary M., Olshan, Andrew F., Reefhuis, Jennita, Romitti, Paul A., Shaw, Gary M., Werler, Martha, Almli, Lynn M., Browne, Marilyn L., Conway, Kristin M., Feldkamp, Marcia L., Finnell, Richard H., Hobbs, Charlotte, Jenkins, Mary M., Moore, Cynthia, Olshan, Andrew F., Reefhuis, Jennita, Keegan, Romitti, Paul A., Shaw, Gary M., Werler, Martha, Bamshad, Michael J., Brody, Lawrence C., Kay, Denise M., McGoldrick, Daniel, Mullikin, James C., Nickerson, Deborah A., Pangilinan, Faith, Sicko, Robert J., Lane, John, Pankratz, Nathan, Bamshad, Michael J., Brody, Lawrence C., Feldkamp, Marcia L., Kay, Denise M., Lane, John, McGoldrick, Daniel, Mills, James L., Nickerson, Deborah A., Pankratz, Nathan, Pitsava, Georgia, Romitti, Paul A., Sicko, Robert J., Pitsava, Georgia, Feldkamp, Marcia L., Kay, Denise M., Lane, John, Mills, James L., Pankratz, Nathan, Pangilinan, Faith, Romitti, Paul A., Almli, Lynn M., Bamshad, Michael J., Brody, Lawrence C., Conway, Kristin M., Cunniff, Chris, Finnell, Richard H., Hobbs, Charlotte, Jenkins, Mary M., McGoldrick, Daniel, Mullikin, James C., Nickerson, Deborah A., Olshan, Andrew F., Reefhuis, Jennita, Keegan, Browne, Marilyn L., Canfield, Shaw, Gary M., Sicko, Robert J., Mills, James L., Romitti, Paul A.

    Veröffentlicht in Birth defects research

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