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 , 7-14.

Akkuş, G., MENZİLETOĞLU YILDIZ, Ş. S., KOCAMAZ, D., EVRAN, M., SERT, M., & TETİKER, B. 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, 7-14.

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, 7-14, 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.7-14, 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.7-14.

@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={7-14} }