akkuş, G. Et Al. 2018. Melanocortin 2 Receptor Mutations and Clinical Significance in Case of Cushing Syndrome and Subclinical Cushing Syndrome and Primary Aldosteronism. INTERNATIONAL JOURNAL OF HUMAN GENETICS , vol.18, no.4 , 259-266.

akkuş, G., Yildiz, Ş. S., KOCAMAZ, D., EVRAN, M., SERT, M., & Tetiker, T., (2018). Melanocortin 2 Receptor Mutations and Clinical Significance in Case of Cushing Syndrome and Subclinical Cushing Syndrome and Primary Aldosteronism. INTERNATIONAL JOURNAL OF HUMAN GENETICS , vol.18, no.4, 259-266.

akkuş, GAMZE Et Al. "Melanocortin 2 Receptor Mutations and Clinical Significance in Case of Cushing Syndrome and Subclinical Cushing Syndrome and Primary Aldosteronism," INTERNATIONAL JOURNAL OF HUMAN GENETICS , vol.18, no.4, 259-266, 2018

akkuş, GAMZE Et Al. "Melanocortin 2 Receptor Mutations and Clinical Significance in Case of Cushing Syndrome and Subclinical Cushing Syndrome and Primary Aldosteronism." INTERNATIONAL JOURNAL OF HUMAN GENETICS , vol.18, no.4, pp.259-266, 2018

akkuş, G. Et Al. (2018) . "Melanocortin 2 Receptor Mutations and Clinical Significance in Case of Cushing Syndrome and Subclinical Cushing Syndrome and Primary Aldosteronism." INTERNATIONAL JOURNAL OF HUMAN GENETICS , vol.18, no.4, pp.259-266.

@article{article, author={GAMZE AKKUŞ Et Al. }, title={Melanocortin 2 Receptor Mutations and Clinical Significance in Case of Cushing Syndrome and Subclinical Cushing Syndrome and Primary Aldosteronism}, journal={INTERNATIONAL JOURNAL OF HUMAN GENETICS}, year=2018, pages={259-266} }