Cite
Behçet's-like syndrome associated with idiopathic CD4+ T-lymphocytopenia, opportunistic infections, and a large population of TCR alpha beta+ CD4- CD8- T cells.
MLA
Venzor, J., et al. “Behçet’s-like Syndrome Associated with Idiopathic CD4+ T-Lymphocytopenia, Opportunistic Infections, and a Large Population of TCR Alpha Beta+ CD4- CD8- T Cells.” The American Journal of the Medical Sciences, vol. 313, no. 4, Apr. 1997, pp. 236–38. EBSCOhost, https://doi.org/10.1097/00000441-199704000-00007.
APA
Venzor, J., Hua, Q., Bressler, R. B., Miranda, C. H., & Huston, D. P. (1997). Behçet’s-like syndrome associated with idiopathic CD4+ T-lymphocytopenia, opportunistic infections, and a large population of TCR alpha beta+ CD4- CD8- T cells. The American Journal of the Medical Sciences, 313(4), 236–238. https://doi.org/10.1097/00000441-199704000-00007
Chicago
Venzor, J, Q Hua, R B Bressler, C H Miranda, and D P Huston. 1997. “Behçet’s-like Syndrome Associated with Idiopathic CD4+ T-Lymphocytopenia, Opportunistic Infections, and a Large Population of TCR Alpha Beta+ CD4- CD8- T Cells.” The American Journal of the Medical Sciences 313 (4): 236–38. doi:10.1097/00000441-199704000-00007.