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Identification of mobile retrocopies during genetic testing: Consequences for routine diagnosis by Chatron, N, Cassinari, K, Quenez, O, Baert-Desurmont, S, Bardel, C, Buisine, M, Calpena, E, Capri, Y, Galbany, J, Diguet, F, Edery, P, Isidor, B, Labalme, A, Le Caignec, C, Lévy, J, Lecoquierre, F, Lindenbaum, P, Pichon, O, Rollat-Farnier, P, Simonet, T, Saugier-Veber, P, Tabet, A, Toutain, A, Wilkie, A, Lesca, G, Sanlaville, D, Nicolas, G, Schluth-Bolard, C
Published 2019Journal article -
2
Clinical spectrum of STX1B-related epileptic disorders by Wolking, S, May, P, Mei, D, Møller, RS, Balestrini, S, Helbig, KL, Altuzarra, CD, Chatron, N, Kaiwar, C, Stöhr, K, Widdess-Walsh, P, Mendelsohn, BA, Numis, A, Cilio, MR, Van Paesschen, W, Svendsen, LL, Oates, S, Hughes, E, Goyal, S, Brown, K, Saenz, M, Dorn, T, Muhle, H, Pagnamenta, AT, Vavoulis, DV, Knight, SJL, Taylor, JC, Canevini, MP, Darra, F, Gavrilova, RH, Powis, Z, Tang, S, Marquetand, J, Armstrong, M, McHale, D, Klee, EW, Kluger, GJ, Lowenstein, DH, Weckhuysen, S, Pal, DK, Helbig, I, Guerrini, R, Thomas, RH, Thomas, RH, Rees, MI, Lesca, G, Sisodiya, SM, Weber, YG, Lal, D, Marini, C, Lerche, H, Schubert, J
Published 2019Journal article