Akcan, N. Et Al. 2017. A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections. FRONTIERS IN ENDOCRINOLOGY , vol.8 .

Akcan, N., SERAKINCI, N., Turkgenc, B., Bundak, R., Bahceciler, N., & Temel, Ş. G., (2017). A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections. FRONTIERS IN ENDOCRINOLOGY , vol.8.

Akcan, Nese Et Al. "A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections," FRONTIERS IN ENDOCRINOLOGY , vol.8, 2017

Akcan, Nese Et Al. "A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections." FRONTIERS IN ENDOCRINOLOGY , vol.8, 2017

Akcan, N. Et Al. (2017) . "A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections." FRONTIERS IN ENDOCRINOLOGY , vol.8.

@article{article, author={Nese Akcan Et Al. }, title={A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections}, journal={FRONTIERS IN ENDOCRINOLOGY}, year=2017}