Treffer 1 - 19 von 19 für Suche 'MCKEE, E.H', Suchdauer: 1,23s Treffer weiter einschränken
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10
  11. 11
  12. 12

    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 Kjaersgaard, 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

    Volltext
    Artikel
  13. 13
  14. 14
  15. 15
  16. 16
  17. 17
  18. 18

    Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP43 inclusions von Van Deerlin, V.M, Sleiman, P.M.A, Martinez-Lage, M, Chen-Plotkin, A, Wang, L.S, Graff-Radford, N.R, Dickson, D.W, Rademakers, R, Boeve, B.F, Grossman, M, Arnold, S.E, Mann, D.M.A, Pickering-Brown, S.M, Seelaar, H, Heutink, P, van Swieten, J.C, Murrell, J.R, Ghetti, B, Spina, S, Grafman, J, Hodges, J, Spillantini, M.G, Gilman, S, Lieberman, A.P, Kaye, J.A, Woltjer, R.L, Bigio, E.H, Mesulam, M, al-Sarraj, S, Troakes, C, Rosenberg, R.N, White, C.L, Ferrer, I, Llado, A, Neumann, M, Kretzschmar, H.A, Hulette, C.M, Welsh-Bohmer, K.A, Miller, B.L, Alzualde, A, de Munain, A.L, McKee, A.C, Gearing, M, Levey, A.I, Lah, J.J, Hardy, J, Rohrer, J.D, Lashley, T, Mackenzie, I.R.A, Feldman, H.H, Hamilton, R.L, Dekosky, S.T, van der Zee, J, Kumar-Singh, S, Van Broeckhoven, C, Mayeux, R, Vonsattel, J.P.G, Troncoso, J.C, Kril, J.J, Kwok, J.B.J, Halliday, G.M, Bird, T.D, Ince, P.G, Shaw, P.J, Cairns, N.J, Morris, J.C, McLean, C.A, DeCarli, C, Ellis, W.G, Freeman, S.H, Frosch, M.P, Growdon, J.H, Perl, D.P, Sano, M, Bennett, D.A, Schneider, J.A, Beach, T.G, Reiman, E.M, Woodruff, B.K, Cummings, J, Vinters, H.V, Miller, C.A, Chui, H.C, Alafuzoff, I, Hartikainen, P, Seilhean, D, Galasko, D, Masliah, E, Cotman, C.W, Tunon, M.T, Martinez, M.C.C, Munoz, D.G, Carroll, S.L, Marson, D, Riederer, P.F, Bogdanovic, N, Schellenberg, G.D, Hakonarson, H, Trojanowski, J.Q, Lee, V.M.Y

    Volltext bestellen
    Artikel
  19. 19