Gilling, M., Dullinger, J. S., Gesk, S., Metzke-Heidemann, S., Siebert, R., Meyer, T., . . . Thomas, N. S. (2006). Breakpoint Cloning and Haplotype Analysis Indicate a Single Origin of the Common Inv(10)(p11.2q21.2) Mutation among Northern Europeans. The American Society of Human Genetics.
Chicago-tyylinen lähdeviittausGilling, Mette, et al. Breakpoint Cloning and Haplotype Analysis Indicate a Single Origin of the Common Inv(10)(p11.2q21.2) Mutation Among Northern Europeans. The American Society of Human Genetics, 2006.
MLA-viiteGilling, Mette, et al. Breakpoint Cloning and Haplotype Analysis Indicate a Single Origin of the Common Inv(10)(p11.2q21.2) Mutation Among Northern Europeans. The American Society of Human Genetics, 2006.
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