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    Modeling COVID-19 scenarios for the United States von Reiner, Robert C., Jr, Barber, Ryan M, Collins, James K, Zheng, Peng, Adolph, Christopher, Albright, James, Antony, Catherine M, Aravkin,Aleksandr Y, Bachmeier, Steven D, Bang-Jensen, Bree, Bannick, Marlena S, Bloom, Sabina, Carter, Austin, Castro, Emma, Causey, Kate, Chakrabarti, Suman, Charlson, Fiona J, Cogen, Rebecca M, Combs, Emily, Dai, Xiaochen, Dangel, William James, Earl, Lucas, Ewald, Samuel B, Maha, Ezalarab, Ferrari, Alize J, Flaxman, Abraham, Frostad, Joseph Jon, Fukllman, Nancy, Gakidou, Emmanuela, Gallagher, John, Glenn, Scott D, Goosmann, Erik A, He, Jiawei, Henry, Nathaniel J, Hulland, Erin N, Hurst, Benjamin, Johanns, Casey, Kendrick, Parkes J, Khemani, Apurva, Larson, Samantha Leigh, Lazzar-Atwood, Alice, LeGrand, Kate E, Lescinsky, Haley, Lindstorm, Akiaja, Linebarger, Emily, Lozano, Rafael, Ma, Rui, Mansson, Johan, Magistro, Beatrice, Mantilla Herrera, Ana M, Marczak, Laurie B, Miller-Petrie, Molly K, Mokdad, Ali H, Morgan, Julia Deryn, Naik, Paulami, Odell, Christopher M, O'Halloran, James K, Osgood-Zimmerman, Aaron E, Ostroff, Samuel M, Pasovic, Maja, Penberthy, Louise, Phipps, Geoffrey, Pigott, David M, Pollock, Ian, Ramshaw, Rebecca E, Redford, Sofia Boston, Reinke, Grace, Rolfe, Sam, Santomauro, Damian Francesco, Shackleton, John R, Shaw, David H, Sheena, Brittney S, Sholokhov, Aleksei, Sorensen, Reed J.D, Sparks, Gianna, Spurlock, Emma Elizabeth, Subart, Michelle L, Syailendrawati, Ruri, Torre, Anna E, Troeger, Christopher E, Vos, Theo, Watson, Alexandrea, Watson, Stefanie, Wiens, Kirsten E, Woyczynski, Lauren, Xu, Liming, Zhang, Jize, Hay, Simon I, Lim, Stephen S, Murray, Christopher J.L

    Veröffentlicht in Nature medicine

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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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