Toraman, B. Et Al. 2013. Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation. GENE , vol.513 , 202-208.

Toraman, B., Okten, A. N., Kalay, E., Karagüzel, G., Dinçer, T., Acıkgoz, E. G., ... Karaguzel, A.(2013). Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation. GENE , vol.513, 202-208.

Toraman, BAYRAM Et Al. "Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation," GENE , vol.513, 202-208, 2013

Toraman, BAYRAM Et Al. "Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation." GENE , vol.513, pp.202-208, 2013

Toraman, B. Et Al. (2013) . "Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation." GENE , vol.513, pp.202-208.

@article{article, author={BAYRAM TORAMAN Et Al. }, title={Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation}, journal={GENE}, year=2013, pages={202-208} }