APA (7. basım) Alıntı

Tuwaijri, A. A., Alyafee, Y., Umair, M., Alsubait, A., Alharbi, M., AlEidi, H., . . . Alfadhel, M. (2023). Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype. Wiley.

Chicago Style (17. basım) Atıf

Tuwaijri, Abeer Al, et al. Congenital Disorder of Glycosylation with Defective Fucosylation 2 (FCSK Gene Defect): The Third Report in the Literature with a Mild Phenotype. Wiley, 2023.

MLA (9th ed.) Atıf

Tuwaijri, Abeer Al, et al. Congenital Disorder of Glycosylation with Defective Fucosylation 2 (FCSK Gene Defect): The Third Report in the Literature with a Mild Phenotype. Wiley, 2023.