Cite
HARVARD Citation
Sun, S. et al. (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), pp. 766-768. [Online].
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Sun, S. et al. (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), pp. 766-768. [Online].