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