Treffer 1 - 20 von 54 für Suche 'Jensen, Rebekah P.', Suchdauer: 1,60s Treffer weiter einschränken
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    Estimating global, regional, and national daily and cumulative infections with SARS-CoV-2 through Nov 14, 2021: a statistical analysis von Barber, Ryan M, Sorensen, Reed J D, Pigott, David M, Bisignano, Catherine, Carter, Austin, Amlag, Joanne O, Collins, James K, Abbafati, Cristiana, Adolph, Christopher, Allorant, Adrien, Aravkin, Aleksandr Y, Bang-Jensen, Bree L, Castro, Emma, Chakrabarti, Suman, Cogen, Rebecca M, Combs, Emily, Comfort, Haley, Cooperrider, Kimberly, Dai, Xiaochen, Daoud, Farah, Deen, Amanda, Earl, Lucas, Erickson, Megan, Ewald, Samuel B, Ferrari, Alize J, Flaxman, Abraham D, Frostad, Joseph Jon, Fullman, Nancy, Giles, John R, Guo, Gaorui, He, Jiawei, Helak, Monika, Hulland, Erin N, Huntley, Bethany M, Lazzar-Atwood, Alice, LeGrand, Kate E, Lim, Stephen S, Lindstrom, Akiaja, Linebarger, Emily, Lozano, Rafael, Magistro, Beatrice, Malta, Deborah Carvalho, Månsson, Johan, Mantilla Herrera, Ana M, Mokdad, Ali H, Monasta, Lorenzo, Naghavi, Mohsen, Nomura, Shuhei, Odell, Christopher M, Olana, Latera Tesfaye, Ostroff, Samuel M, Pasovic, Maja, Pease, Spencer A, Reiner Jr, Robert C, Reinke, Grace, Ribeiro, Antonio Luiz P, Santomauro, Damian F, Sholokhov, Aleksei, Spurlock, Emma E, Syailendrawati, Ruri, Topor-Madry, Roman, Vo, Anh Truc, Vos, Theo, Walcott, Rebecca, Walker, Ally, Wiens, Kirsten E, Wiysonge, Charles Shey, Worku, Nahom Alemseged, Zheng, Peng, Hay, Simon I, Gakidou, Emmanuela, Murray, Christopher J L

    Veröffentlicht in The Lancet (British edition)

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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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