APA استشهاد

Thomas, R., Sanna-Cherchi, S., Warady, B. A., Furth, S. L., Kaskel, F. J., & Gharavi, A. G. (2011). HNF1B and PAX2 mutations are a Common Cause of Renal Hypodysplasia in the CKiD Cohort.

استشهاد بنمط شيكاغو

Thomas, Rosemary, Simone Sanna-Cherchi, Bradley A. Warady, Susan L. Furth, Frederick J. Kaskel, و Ali G. Gharavi. HNF1B and PAX2 Mutations Are a Common Cause of Renal Hypodysplasia in the CKiD Cohort. 2011.

MLA استشهاد

Thomas, Rosemary, et al. HNF1B and PAX2 Mutations Are a Common Cause of Renal Hypodysplasia in the CKiD Cohort. 2011.

تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.