Treffer 1 - 20 von 29 für Suche 'Snyder, Holly K', Suchdauer: 1,50s Treffer weiter einschränken
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    SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research von Feliciano, Pamela, Daniels, Amy M., Esler, Amy, Gutierrez, Anibal, Nicholson, Amy, Stephens, Alexandra N., Stedman, Amy, Finucane, Brenda, O’Roak, Brian J., Robertson, Beverly E., Rodriguez, Barbara, Van Metre, Bonnie, Bradley, Catherine, Erickson, Craig A., Harkins, Christina, Ochoa-Lubinoff, Cesar, Rosenberg, Cordelia R., Smith, Christopher J., Taylor, Cora M., White, Loran Casey, Walston, Corrie H., Amaral, David G., Coury, Daniel Lee, Sarver, Dustin E., Li, Deana, Berry-Kravis, Elizabeth, Fombonne, Eric J., Hofammann, Eugenia, Wodka, Ericka L., O’Connor, Eirene, Miller, Fiona, Stein, Gail, Hutter, Hanna, Li, Hai, Lechniak, Holly, Schneider, Hoa Lam, Zaydens, Hana, Arriaga, Ivette, Cubells, Joseph F., Cordova, Jeanette M., Gunderson, Jaclyn, McCracken, James T., Michaelson, Jacob J., Neely, Jason, Orobio, Jessica, Piven, Joseph, Tjernagel, Jennifer, Dent, Katherine, Schweers, Kathryn A., Law, J. Kiely, Lowe, Kathryn, O’Brien, Kaela, Smith, Kaitlin, Pawlowski, Katherine G., Pierce, Karen L., Roeder, Katherine, Coppola, Leigh A., Carpenter, Laura, Huang-Storms, Lark Y., Herbert, Lynette M., Simon, Laura, Soorya, Latha V., Wasserburg, Lucy, Lazar, Maya, Currin, Mary Hannah, Heyman, Michelle, Jones, Mark, Jordy, Michelle, Sahin, Mustafa, Siegel, Matthew S., Yinger, Meredith, Hanna, Nathan, Juarez, A. Pablo, Remington, Rick, Schultz, Robert T., Carpenter, Sarah, Eldred, Sara, Francis, Sunday, Horner, Susannah, Lee, Soo J., Mastel, Sarah A., Myers, Vincent J., Amatya, Alpha, Chatha, Ahmad S., Lash, Alex E., Ridenour, Curtis, Stock, Colleen M., Schmidt, Danielle, Butler, Martin E., Carriero, Nicholas, Volfovsky, Natalia, Edgar, Ron, Chin, Wubin, Jensen, William, Krentz, Anthony D., Astrovskaya, Irina, Gibbs, Richard A., Han, Xinwei, Shen, Yufeng, Reichardt, Louis F.

    Veröffentlicht in Neuron (Cambridge, Mass.)

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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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