Einträge von Moore, A. T. auf dem Publikationsserver

Sofat, R., Casas, J. P., Webster, A. R., Bird, A. C., Mann, S. S., Yates, J. R., Moore, A. T., Sepp, T., Cipriani, V. , Bunce, C. , Khan, J. C., Shahid, H., Swaroop, A. , Abecasis, G. , Branham, K. E., Zareparsi, S., Bergen, A. A., Klaver, C. C. , Baas, D. C., Zhang, K., Chen, Y., Gibbs, D., Weber, Bernhard H. F. , et, al., make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference und make_name_string expected hash reference (2012) Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype. International Journal of Epidemiology 41 (1), S. 250-262. Volltext nicht vorhanden.

Kelsell, R. E., Gregory-Evans, K., Gregory-Evans, C. Y., Holder, G. E., Jay, M. R., Weber, Bernhard H. F. , Moore, A. T., Bird, A. C. und Hunt, D. M. (1998) Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q. The American Journal of Human Genetics 63 (1), S. 274-279. Volltext nicht vorhanden.