APA (7th ed.) Citation

Ordóñez, T. B., Mesa, T. C., Cruz, P. L., Navarro, A. d. J. G., & Reyes, T. E. Detection of the I172N Mutation in Cuban Patients with Congenital Adrenal Hyperplasia due to 21 Hydroxylase Insufficiency. Universidad de las Ciencias Médicas de Cienfuegos.

Chicago Style (17th ed.) Citation

Ordóñez, Taimí Barrueta, Teresa Collazo Mesa, Paulina Lantigua Cruz, Adrián de Jesús González Navarro, and Tania Espinosa Reyes. Detection of the I172N Mutation in Cuban Patients with Congenital Adrenal Hyperplasia Due to 21 Hydroxylase Insufficiency. Universidad de las Ciencias Médicas de Cienfuegos.

MLA (9th ed.) Citation

Ordóñez, Taimí Barrueta, et al. Detection of the I172N Mutation in Cuban Patients with Congenital Adrenal Hyperplasia Due to 21 Hydroxylase Insufficiency. Universidad de las Ciencias Médicas de Cienfuegos.