Cita APA

Aycan, Z., Cangul, H., Muzza, M., Bas, V. N., Fugazzola, L., Chatterjee, V. K., . . . Schoenmakers, N. (2017). Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism. J Clin Endocrinol Metab.

Citación estilo Chicago

Aycan, Zehra, Hakan Cangul, Marina Muzza, Veysel N. Bas, Laura Fugazzola, V. Krishna Chatterjee, Luca Persani, y Nadia Schoenmakers. "Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism." J Clin Endocrinol Metab 2017.

Cita MLA

Aycan, Zehra, et al. "Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism." J Clin Endocrinol Metab 2017.