Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.

MLA

Vathipadiekal, Vinod, et al. “Homozygosity for a Haplotype in the HBG2-OR51B4 Region Is Exclusive to Arab-Indian Haplotype Sickle Cell Anemia.” American Journal of Hematology, vol. 91, no. 6, June 2016, pp. E308–11. EBSCOhost, https://doi.org/10.1002/ajh.24368.

APA

Vathipadiekal, V., Alsultan, A., Baltrusaitis, K., Farrell, J. J., Al-Rubaish, A. M., Al-Muhanna, F., Naserullah, Z., Suliman, A., Patra, P. K., Milton, J. N., Farrer, L. A., Chui, D. H. K., Al-Ali, A. K., Sebastiani, P., & Steinberg, M. H. (2016). Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia. American Journal of Hematology, 91(6), E308–E311. https://doi.org/10.1002/ajh.24368

Chicago

Vathipadiekal, Vinod, Abdulrahman Alsultan, Kristin Baltrusaitis, John J. Farrell, Abdullah M. Al-Rubaish, Fahad Al-Muhanna, Zaki Naserullah, et al. 2016. “Homozygosity for a Haplotype in the HBG2-OR51B4 Region Is Exclusive to Arab-Indian Haplotype Sickle Cell Anemia.” American Journal of Hematology 91 (6): E308–11. doi:10.1002/ajh.24368.