Lettre, G., Sankaran, V. G., Bezerra, M. A. C., Araújo, A. S., Uda, M., Sanna, S., . . . Orkin, S. H. (2008). DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proceedings of the National Academy of Sciences - PNAS, 105(33), 11869. https://doi.org/10.1073/pnas.0804799105
Citace podle Chicago (17th ed.)Lettre, Guillaume, et al. "DNA Polymorphisms at the BCL11A, HBS1L-MYB, and Beta-globin Loci Associate with Fetal Hemoglobin Levels and Pain Crises in Sickle Cell Disease." Proceedings of the National Academy of Sciences - PNAS 105, no. 33 (2008): 11869. https://doi.org/10.1073/pnas.0804799105.
Citace podle MLA (9th ed.)Lettre, Guillaume, et al. "DNA Polymorphisms at the BCL11A, HBS1L-MYB, and Beta-globin Loci Associate with Fetal Hemoglobin Levels and Pain Crises in Sickle Cell Disease." Proceedings of the National Academy of Sciences - PNAS, vol. 105, no. 33, 2008, p. 11869, https://doi.org/10.1073/pnas.0804799105.