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HARVARD Citation
Elliott, A. et al. (2013). A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort. Journal of medical genetics. 50 (12), pp. 819-822. [Online].
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Elliott, A. et al. (2013). A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort. Journal of medical genetics. 50 (12), pp. 819-822. [Online].