Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Den, L. v."'
Autor:
Steinberg, S., Jong, S. d., Genomics, I. S., Andreassen, O. A., Werge, T., Børglum, A. D., Mors, O., Mortensen, P. B., Gustafsson, O., Costas, J., O. P. H., Demontis, D., Papiol, S., Huttenlocher, J., Mattheisen, M., Breuer, R., Vassos, E., Giegling, I., Fraser, G., Walker, N., Tuulio Henriksson, A., Suvisaari, J., Lönnqvist, J., Paunio, T., Agartz, I., Melle, I., Djurovic, S., Strengman, E., G. R. O., Jürgens, G., Glenthøj, B., Terenius, L., Hougaard, D. M., Orntoft, T., Wiuf, C., Didriksen, M., Hollegaard, M. V., Nordentoft, M., Winkel, R. v., Kenis, G., Abramova, L., Kaleda, V., Arrojo, M., Sanjuán, J., Arango, C., Sperling, S., Rossner, M., Ribolsi, M., Magni, V., Siracusano, A., Christiansen, C., Kiemeney, L. A., Veldink, J., Den, L. v., Ingason, A., Muglia, P., Murray, R., Nöthen, M. M., Sigurdsson, E., Petursson, H., Thorsteinsdottir, U., Kong, A., Rubino, I. A., Hert, M. D., Réthelyi, J. M., Bitter, I., Jönsson, E. G., Golimbet, V., Carracedo, A., Ehrenreich, H., Craddock, N., Owen, M. J., O'Donovan, M. C., Case, W. T., Ruggeri, Mirella, Tosato, Sarah, Peltonen, L., Ophoff, R. A., Collier, D. A., Clair, D. S., Rietschel, M., Cichon, S., Stefansson, H., Rujescu, D., Stefansson, K.
Publikováno v:
Human Molecular Genetics Vol. 20 Issue 20: pp. 4076-4081
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
Human Molecular Genetics
Human molecular genetics 20, 4076-4081 (2011). doi:10.1093/hmg/ddr325
Human Molecular Genetics, 20, 20, pp. 4076-81
Human Molecular Genetics, 20, 4076-81
Human Molecular Genetics, 20(20), 4076-4081. Oxford University Press
Human molecular genetics, 20(20), 4076-4081. Oxford University Press
Human Molecular Genetics; Vol 20
Steinberg, S, de Jong, S, Andreassen, O A, Werge, T, Børglum, A D, Mors, O, Mortensen, P B, Gustafsson, O, Costas, J, Pietiläinen, O P H, Demontis, D, Papiol, S, Huttenlocher, J, Mattheisen, M, Breuer, R, Vassos, E, Giegling, I, Fraser, G, Walker, N, Tuulio-Henriksson, A, Suvisaari, J, Lönnqvist, J, Paunio, T, Agartz, I, Melle, I, Djurovic, S, Strengman, E, Jürgens, G, Glenthøj, B, Terenius, L, Hougaard, D M, Orntoft, T, Wiuf, C, Didriksen, M, Hollegaard, M V, Nordentoft, M, van Winkel, R, Kenis, G, Abramova, L, Kaleda, V, Arrojo, M, Sanjuán, J, Arango, C, Sperling, S, Rossner, M, Ribolsi, M, Magni, V, Siracusano, A, Christiansen, C, Kiemeney, L A & Irish Schizophrenia Genomics Consortium 2011, ' Common Variants at VRK2 and TCF4 Conferring Risk of Schizophrenia ', Human Molecular Genetics, vol. 20, no. 20, pp. 4076-81 . https://doi.org/10.1093/hmg/ddr325
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
Human Molecular Genetics
Human molecular genetics 20, 4076-4081 (2011). doi:10.1093/hmg/ddr325
Human Molecular Genetics, 20, 20, pp. 4076-81
Human Molecular Genetics, 20, 4076-81
Human Molecular Genetics, 20(20), 4076-4081. Oxford University Press
Human molecular genetics, 20(20), 4076-4081. Oxford University Press
Human Molecular Genetics; Vol 20
Steinberg, S, de Jong, S, Andreassen, O A, Werge, T, Børglum, A D, Mors, O, Mortensen, P B, Gustafsson, O, Costas, J, Pietiläinen, O P H, Demontis, D, Papiol, S, Huttenlocher, J, Mattheisen, M, Breuer, R, Vassos, E, Giegling, I, Fraser, G, Walker, N, Tuulio-Henriksson, A, Suvisaari, J, Lönnqvist, J, Paunio, T, Agartz, I, Melle, I, Djurovic, S, Strengman, E, Jürgens, G, Glenthøj, B, Terenius, L, Hougaard, D M, Orntoft, T, Wiuf, C, Didriksen, M, Hollegaard, M V, Nordentoft, M, van Winkel, R, Kenis, G, Abramova, L, Kaleda, V, Arrojo, M, Sanjuán, J, Arango, C, Sperling, S, Rossner, M, Ribolsi, M, Magni, V, Siracusano, A, Christiansen, C, Kiemeney, L A & Irish Schizophrenia Genomics Consortium 2011, ' Common Variants at VRK2 and TCF4 Conferring Risk of Schizophrenia ', Human Molecular Genetics, vol. 20, no. 20, pp. 4076-81 . https://doi.org/10.1093/hmg/ddr325
To access publisher full text version of this article. Please click on the hyperlink in Additional Links field. Common sequence variants have recently joined rare structural polymorphisms as genetic factors with strong evidence for association with s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e6c75c570a1866902c4a034d4600beb
http://hdl.handle.net/10550/44673
http://hdl.handle.net/10550/44673