Prevalence of CAH-X Syndrome in Italian Patients with Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency.

MLA

Paragliola, Rosa Maria, et al. “Prevalence of CAH-X Syndrome in Italian Patients with Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency.” Journal of Clinical Medicine, vol. 11, no. 13, July 2022, p. 3818–N.PAG. EBSCOhost, https://doi.org/10.3390/jcm11133818.

APA

Paragliola, R. M., Perrucci, A., Foca, L., Urbani, A., & Concolino, P. (2022). Prevalence of CAH-X Syndrome in Italian Patients with Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency. Journal of Clinical Medicine, 11(13), 3818–N.PAG. https://doi.org/10.3390/jcm11133818

Chicago

Paragliola, Rosa Maria, Alessia Perrucci, Laura Foca, Andrea Urbani, and Paola Concolino. 2022. “Prevalence of CAH-X Syndrome in Italian Patients with Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency.” Journal of Clinical Medicine 11 (13): 3818–N.PAG. doi:10.3390/jcm11133818.