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Stranneheim H, Lagerstedt-Robinson K, Magnusson M, et al. Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients. Genome Med. 2021;13(1):40doi: 10.1186/s13073-021-00855-5.
Stranneheim, H., Lagerstedt-Robinson, K., Magnusson, M., Kvarnung, M., Nilsson, D., Lesko, N., Engvall, M., Anderlid, B. M., Arnell, H., Johansson, C. B., Barbaro, M., Björck, E., Bruhn, H., Eisfeldt, J., Freyer, C., Grigelioniene, G., Gustavsson, P., Hammarsjö, A., Hellström-Pigg, M., Iwarsson, E., Jemt, A., Laaksonen, M., Enoksson, S. L., Malmgren, H., Naess, K., Nordenskjöld, M., Oscarson, M., Pettersson, M., Rasi, C., Rosenbaum, A., Sahlin, E., Sardh, E., Stödberg, T., Tesi, B., Tham, E., Thonberg, H., Töhönen, V., von Döbeln, U., Vassiliou, D., Vonlanthen, S., Wikström, A. C., Wincent, J., Winqvist, O., Wredenberg, A., Ygberg, S., Zetterström, R. H., Marits, P., Soller, M. J., Nordgren, A., Wirta, V., Lindstrand, A., & Wedell, A. (2021). Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients. Genome medicine, 13(1), 40. https://doi.org/10.1186/s13073-021-00855-5
Stranneheim, Henrik, et al. "Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients." Genome medicine vol. 13,1 (2021): 40. doi: https://doi.org/10.1186/s13073-021-00855-5
Stranneheim H, Lagerstedt-Robinson K, Magnusson M, Kvarnung M, Nilsson D, Lesko N, Engvall M, Anderlid BM, Arnell H, Johansson CB, Barbaro M, Björck E, Bruhn H, Eisfeldt J, Freyer C, Grigelioniene G, Gustavsson P, Hammarsjö A, Hellström-Pigg M, Iwarsson E, Jemt A, Laaksonen M, Enoksson SL, Malmgren H, Naess K, Nordenskjöld M, Oscarson M, Pettersson M, Rasi C, Rosenbaum A, Sahlin E, Sardh E, Stödberg T, Tesi B, Tham E, Thonberg H, Töhönen V, von Döbeln U, Vassiliou D, Vonlanthen S, Wikström AC, Wincent J, Winqvist O, Wredenberg A, Ygberg S, Zetterström RH, Marits P, Soller MJ, Nordgren A, Wirta V, Lindstrand A, Wedell A. Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients. Genome Med. 2021 Mar 17;13(1):40. doi: 10.1186/s13073-021-00855-5. PMID: 33726816; PMCID: PMC7968334.
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