APA (7th ed.) Citation

Shlien, A., Tabori, U., Marshall, C. R., Pienkowska, M., Feuk, L., Novokmet, A., . . . Malkin, D. (2008). Excessive genomic DNA copy number variation in the L1—Fraumeni cancer predisposition syndrome. Proceedings of the National Academy of Sciences of the United States of America, 105(32), 11264. https://doi.org/10.1073/pnas.0802970105

Chicago Style (17th ed.) Citation

Shlien, Adam, et al. "Excessive Genomic DNA Copy Number Variation in the L1—Fraumeni Cancer Predisposition Syndrome." Proceedings of the National Academy of Sciences of the United States of America 105, no. 32 (2008): 11264. https://doi.org/10.1073/pnas.0802970105.

MLA (9th ed.) Citation

Shlien, Adam, et al. "Excessive Genomic DNA Copy Number Variation in the L1—Fraumeni Cancer Predisposition Syndrome." Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 32, 2008, p. 11264, https://doi.org/10.1073/pnas.0802970105.