Foulkes, W. D., Thiffault, I., Gruber, S. B., Horwitz, M., Hamel, N., Lee, C., . . . Ellis, N. A. (2002). The Founder Mutation MSH2*1906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population. The American Society of Human Genetics.
Citação norma ChicagoFoulkes, W. D., et al. The Founder Mutation MSH2*1906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population. The American Society of Human Genetics, 2002.
MLA citiranjeFoulkes, W. D., et al. The Founder Mutation MSH2*1906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population. The American Society of Human Genetics, 2002.
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