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.
توثيق أسلوب شيكاغو (الطبعة السابعة عشر)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.
توثيق جمعية اللغة المعاصرة MLA (الإصدار التاسع)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.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.