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APA Citation
Sun, S., Greenwood, C. M. T., Thiffault, I., Hamel, N., Chong, G., & Foulkes, W. D. (2005). the HNPCC associated MSH2*1906G→C founder mutation probably originated between 1440 CE and 1715 CE in the Ashkenazi Jewish population. Journal of medical genetics, 42(10), 766–768. http://access.bl.uk/ark:/81055/vdc_100135556635.0x00003e