APA Alıntı

Sly, W. S., Hewett-Emmett, D., Whyte, M. P., Yu, Y. S., & Tashian, R. E. (1983). Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.

Chicago Stili Alıntı

Sly, W S., D. Hewett-Emmett, M P. Whyte, Y S. Yu, ve R E. Tashian. Carbonic Anhydrase II Deficiency Identified As the Primary Defect in the Autosomal Recessive Syndrome of Osteopetrosis With Renal Tubular Acidosis and Cerebral Calcification. 1983.

MLA Alıntı

Sly, W S., et al. Carbonic Anhydrase II Deficiency Identified As the Primary Defect in the Autosomal Recessive Syndrome of Osteopetrosis With Renal Tubular Acidosis and Cerebral Calcification. 1983.