APA (7th ed.) Citation

Mohamadsalih, G., Bureshad, K. A., Mohammed, I., Chirayath, S., Hamdoun, E., & Hussain, K. Permanent Congenital Hypothyroidism due to Rare Thyroglobulin Gene Variant (p.Cys1476Arg): A Delayed Diagnosis of Thyroid Dyshormonogenesis. Wiley.

Chicago Style (17th ed.) Citation

Mohamadsalih, Ghassan, Khalid Al Bureshad, Idris Mohammed, Shiga Chirayath, Elwaseila Hamdoun, and Khalid Hussain. Permanent Congenital Hypothyroidism Due to Rare Thyroglobulin Gene Variant (p.Cys1476Arg): A Delayed Diagnosis of Thyroid Dyshormonogenesis. Wiley.

MLA (9th ed.) Citation

Mohamadsalih, Ghassan, et al. Permanent Congenital Hypothyroidism Due to Rare Thyroglobulin Gene Variant (p.Cys1476Arg): A Delayed Diagnosis of Thyroid Dyshormonogenesis. Wiley.