Kardelen, A. D. Et Al. 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. Journal of clinical research in pediatric endocrinology , vol.10, no.3 , 206-215.

Kardelen, A. D., Toksoy, G., Bas, F., Abali, Z. Y., Gencay, G., Poyrazoglu, S., ... Bundak, R.(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. Journal of clinical research in pediatric endocrinology , vol.10, no.3, 206-215.

Kardelen, Asli 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," Journal of clinical research in pediatric endocrinology , vol.10, no.3, 206-215, 2018

Kardelen, Asli D. 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." Journal of clinical research in pediatric endocrinology , vol.10, no.3, pp.206-215, 2018

Kardelen, A. D. Et Al. (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." Journal of clinical research in pediatric endocrinology , vol.10, no.3, pp.206-215.

@article{article, author={Asli Derya Kardelen Et Al. }, title={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}, journal={Journal of clinical research in pediatric endocrinology}, year=2018, pages={206-215} }