Kardelen, A. D., Toksoy, G., Baş, F., Yavaş Abalı, Z., Gençay, G., Poyrazoğlu, Ş., . . . Darendeliler, F. (2018). A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations. J Clin Res Pediatr Endocrinol.
Chicago-tyylinen lähdeviittausKardelen, Aslı Derya, et al. "A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients With 17-Hydroxylase Deficiency Including Two Novel Mutations." J Clin Res Pediatr Endocrinol 2018.
MLA-viiteKardelen, Aslı Derya, et al. "A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients With 17-Hydroxylase Deficiency Including Two Novel Mutations." J Clin Res Pediatr Endocrinol 2018.