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van Riel E, Ausems MG, Hogervorst FB, et al. A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome. Hered Cancer Clin Pract. 2010;8(1):7doi: 10.1186/1897-4287-8-7.
van Riel, E., Ausems, M. G., Hogervorst, F. B., Kluijt, I., van Gijn, M. E., van Echtelt, J., Scheidel-Jacobse, K., Hennekam, E. F., Stulp, R. P., Vos, Y. J., Offerhaus, G. J., Menko, F. H., & Gille, J. J. (2010). A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome. Hereditary cancer in clinical practice, 8(1), 7. https://doi.org/10.1186/1897-4287-8-7
van Riel, Els, et al. "A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome." Hereditary cancer in clinical practice vol. 8,1 (2010): 7. doi: https://doi.org/10.1186/1897-4287-8-7
van Riel E, Ausems MG, Hogervorst FB, Kluijt I, van Gijn ME, van Echtelt J, Scheidel-Jacobse K, Hennekam EF, Stulp RP, Vos YJ, Offerhaus GJ, Menko FH, Gille JJ. A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome. Hered Cancer Clin Pract. 2010 Aug 12;8(1):7. doi: 10.1186/1897-4287-8-7. PMID: 20704743; PMCID: PMC2927519.
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