Ahmad, N., Bahasan, M., Al-Ghamdi, B. A. A., Al-Enizi, H. F., & Al-Zahrani, A. S. (2017). Neonatal severe hyperparathyroidism secondary to a novel homozygous CASR gene mutation. Clin Cases Miner Bone Metab.
Chicago Style aipamenaAhmad, Noman, Mona Bahasan, Balgees Abdulhadi Abdullah Al-Ghamdi, Halah Faleh Al-Enizi, and Ali Saeed Al-Zahrani. "Neonatal Severe Hyperparathyroidism Secondary to a Novel Homozygous CASR Gene Mutation." Clin Cases Miner Bone Metab 2017.
MLA aipamenaAhmad, Noman, et al. "Neonatal Severe Hyperparathyroidism Secondary to a Novel Homozygous CASR Gene Mutation." Clin Cases Miner Bone Metab 2017.
Kontuz: berrikusi erreferentzia hauek erabili aurretik.