APA-viite

Espinosa Reyes, T. M., Collazo Mesa, T., Lantigua Cruz, P. A., Agramonte Machado, A., Domínguez Alonso, E., & Falhammar, H. (2020). Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. BMC Endocr Disord.

Chicago-tyylinen lähdeviittaus

Espinosa Reyes, Tania Mayvel, Teresa Collazo Mesa, Paulina Arasely Lantigua Cruz, Adriana Agramonte Machado, Emma Domínguez Alonso, ja Henrik Falhammar. "Molecular Diagnosis of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency." BMC Endocr Disord 2020.

MLA-viite

Espinosa Reyes, Tania Mayvel, et al. "Molecular Diagnosis of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency." BMC Endocr Disord 2020.

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