Turan, H. Et Al. 2021. Clinical and genetic characteristics of patients with corticosterone methyloxidase deficiency type 2: Novel mutations in cyp11b2. JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.13, no.2 , 232-238.

Turan, H., Çakır, A. D., Özer, Y., Tarçın, G., Özcabi, B., CEYLANER, S., ... ERCAN, O.(2021). Clinical and genetic characteristics of patients with corticosterone methyloxidase deficiency type 2: Novel mutations in cyp11b2. JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.13, no.2, 232-238.

Turan, Hande Et Al. "Clinical and genetic characteristics of patients with corticosterone methyloxidase deficiency type 2: Novel mutations in cyp11b2," JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.13, no.2, 232-238, 2021

Turan, Hande Et Al. "Clinical and genetic characteristics of patients with corticosterone methyloxidase deficiency type 2: Novel mutations in cyp11b2." JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.13, no.2, pp.232-238, 2021

Turan, H. Et Al. (2021) . "Clinical and genetic characteristics of patients with corticosterone methyloxidase deficiency type 2: Novel mutations in cyp11b2." JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.13, no.2, pp.232-238.

@article{article, author={Hande Turan Et Al. }, title={Clinical and genetic characteristics of patients with corticosterone methyloxidase deficiency type 2: Novel mutations in cyp11b2}, journal={JCRPE Journal of Clinical Research in Pediatric Endocrinology}, year=2021, pages={232-238} }