Treffer 1 - 20 von 45 für Suche 'TAYLOR LEONARD GORDON', Suchdauer: 1,20s Treffer weiter einschränken
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    Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders von Gillentine, Madelyn A, Wang, Tianyun, Hoekzema, Kendra, Rosenfeld, Jill, Liu, Pengfei, Guo, Hui, Kim, Chang N, De Vries, Bert B A, Vissers, Lisenka E L M, Nordenskjold, Magnus, Kvarnung, Malin, Lindstrand, Anna, Nordgren, Ann, Gecz, Jozef, Iascone, Maria, Cereda, Anna, Scatigno, Agnese, Maitz, Silvia, Zanni, Ginevra, Bertini, Enrico, Zweier, Christiane, Schuhmann, Sarah, Wiesener, Antje, Pepper, Micah, Panjwani, Heena, Torti, Erin, Abid, Farida, Anselm, Irina, Srivastava, Siddharth, Atwal, Paldeep, Bacino, Carlos A, Bhat, Gifty, Cobian, Katherine, Bird, Lynne M, Friedman, Jennifer, Wright, Meredith S, Callewaert, Bert, Petit, Florence, Mathieu, Sophie, Afenjar, Alexandra, Christensen, Celenie K, White, Kerry M, Elpeleg, Orly, Berger, Itai, Espineli, Edward J, Fagerberg, Christina, Brasch-Andersen, Charlotte, Hansen, Lars Kjærsgaard, Feyma, Timothy, Hughes, Susan, Thiffault, Isabelle, Sullivan, Bonnie, Yan, Shuang, Keller, Kory, Keren, Boris, Mignot, Cyril, Kooy, Frank, Meuwissen, Marije, Basinger, Alice, Kukolich, Mary, Philips, Meredith, Ortega, Lucia, Drummond-Borg, Margaret, Lauridsen, Mathilde, Sorensen, Kristina, Lehman, Anna, Lopez-Rangel, Elena, Levy, Paul, Lessel, Davor, Lotze, Timothy, Madan-Khetarpal, Suneeta, Sebastian, Jessica, Vento, Jodie, Vats, Divya, Benman, L Manace, Mckee, Shane, Mirzaa, Ghayda M, Muss, Candace, Pappas, John, Peeters, Hilde, Romano, Corrado, Elia, Maurizio, Galesi, Ornella, Simon, Marleen E H, van Gassen, Koen L I, Simpson, Kara, Stratton, Robert, Syed, Sabeen, Thevenon, Julien, Palafoll, Irene Valenzuela, Vitobello, Antonio, Bournez, Marie, Faivre, Laurence, Xia, Kun, Earl, Rachel K, Nowakowski, Tomasz, Bernier, Raphael A, Eichler, Evan E

    Veröffentlicht in Genome medicine

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    Expression quantitative trait locus fine mapping of the 17q12–21 asthma locus in African American children: a genetic association and gene expression study von McKennan, Chris G, Bacharier, Leonard B, Hartert, Tina, Johnson, Christine C, Kattan, Meyer, Lemanske, Robert F, Lynch, Susan V, O'Connor, George T, Wegienka, Ganesa, Zoratti, Edward M, Levin, Albert M, Akkerman, Nonna, Aubuchon, Mary Ann, Barone, Charles, Becker, Patrice, Bednarek, Alyssa, Bendixsen, Casper G., Biagini Myers, Jocelyn M., Bobbitt, Kevin, Bochkov, Yury, Bourgeois, Karen, Brockman-Schneider, Rebecca, Burkle, Jeffrey W., Campbell, Janice, Cassidy-Bushrow, Andrea, Chappell, James D., Chasman, Deborah, Connolly, Alexandra, Cootauco, Michelle, Crisafi, Gina, Cruikshank, William, Davidson, Brent, Dixon, Samara, Donnerbauer, Erin, Dresen, Amy, Durrange, Janet, Erickson, Heidi, Ezell, Jerel, Filardo-Collins, Roxanne, Finazzo, Salvatore, Frome, Wayne, Gammell, Rebecca, Gangnon, Ronald E., Gebretsadik, Tebeb, Gibson, Heike, Halonen, Marilyn, Hartert, Tina V., Herbstman, Julie, Hoepner, Lori, Jones, Amelia, Keidel, Kristina, Keifer, Matthew C., Khurana Hershey, Gurgit K., Kim, Haejin, Koerkenmeier, Clint, Lemanske, Jr, Robert F., Liu, Xinhua, Lopez, Silvia, Lothrop, Nathan, Lynch, Susan, Mann, Erik, McCauley, Katherine, McKennon, Chris G., Meece, Jennifer, Miller, Rachel L., Mitchell, Herman, Morgan, Wayne, Nicolae, Daniel, O'Connor, George, O'Toole, Sharon, Pappas, Tressa, Perera, Frederica, Pierce, Marcela, Renneberg, Megan, Riley, Kylie, Roberg, Kathy, Sadovsky, Yoel, Schwartz, Joel, Seroogy, Christine M., Shilts, Meghan H., Sorkness, Ronald, Sperling, Rhoda, Stern, Debra A., Stoffel, Brandy, Strauchman Boyer, Cathey, Tang, Zhengzheng, Tisler, Christopher, Togias, Alkis, Turi, Kedir, Tuzova, Marina, Vrtis, Rose, Wang, Lena, Williams, L. Keoki, Wood, Robert A., Woodcroft, Kimberley, Wright, Rosalind, Zanobetti, Antonella, Zhang, Shirley, Zook, Patricia, Zoratti, Edward M.

    Veröffentlicht in The lancet respiratory medicine

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