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    Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1 von Crow, Yanick J, Chase, Diana S, Lowenstein Schmidt, Johanna, Szynkiewicz, Marcin, Forte, Gabriella M.A, Gornall, Hannah L, Oojageer, Anthony, Anderson, Beverley, Pizzino, Amy, Helman, Guy, Abdel-Hamid, Mohamed S, Abdel-Salam, Ghada M, Ackroyd, Sam, Aeby, Alec, Agosta, Guillermo, Albin, Catherine, Allon-Shalev, Stavit, Arellano, Montse, Ariaudo, Giada, Aswani, Vijay, Babul-Hirji, Riyana, Baildam, Eileen M, Bahi-Buisson, Nadia, Bailey, Kathryn M, Barnerias, Christine, Barth, Magalie, Battini, Roberta, Beresford, Michael W, Bernard, Geneviève, Bianchi, Marika, Billette de Villemeur, Thierry, Blair, Edward M, Bloom, Miriam, Burlina, Alberto B, Luisa Carpanelli, Maria, Carvalho, Daniel R, Castro-Gago, Manuel, Cavallini, Anna, Cereda, Cristina, Chandler, Kate E, Chitayat, David A, Collins, Abigail E, Sierra Corcoles, Concepcion, Cordeiro, Nuno J.V, Crichiutti, Giovanni, Dabydeen, Lyvia, Dale, Russell C, D Arrigo, Stefano, De Goede, Christian G.E.L, De Laet, Corinne, De Waele, Liesbeth, Denzler, Ines, Desguerre, Isabelle, Devriendt, Koenraad, Di Rocco, Maja, Fahey, Michael C, Fazzi, Elisa, Ferrie, Colin D, Figueiredo, António, Gener, Blanca, Goizet, Cyril, Gowrinathan, Nirmala R, Gowrishankar, Kalpana, Hanrahan, Donncha, Isidor, Bertrand, Kara, Bülent, Khan, Nasaim, King, Mary D, Kirk, Edwin P, Kumar, Ram, Lagae, Lieven, Landrieu, Pierre, Lauffer, Heinz, Laugel, Vincent, Piana, Roberta La, Lim, Ming J, Lin, Jean-Pierre S.-M, Linnankivi, Tarja, Mackay, Mark T, Marom, Daphna R, Marques Lourenço, Charles, McKee, Shane A, Moroni, Isabella, Morton, Jenny E.V, Moutard, Marie-Laure, Murray, Kevin, Nabbout, Rima, Nampoothiri, Sheela, Nunez-Enamorado, Noemi, Oades, Patrick J, Olivieri, Ivana, Ostergaard, John R, Pérez-Dueñas, Belén, Prendiville, Julie S, Ramesh, Venkateswaran, Rasmussen, Magnhild, Régal, Luc, Ricci, Federica, Rio, Marlène, Rodriguez, Diana


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