Aghayeva, A. Et Al. 2019. Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency. 58th Annual ESPE meeting , 361-362.

Aghayeva, A., Turan, H., Toksoy, G., Cakir, A. D., Berkay, E., Gunes, N., ... Evliyaoglu, O.(2019). Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency . 58th Annual ESPE meeting (pp.361-362).

Aghayeva, Asmar Et Al. "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency," 58th Annual ESPE meeting, 2019

Aghayeva, Asmar Et Al. "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency." 58th Annual ESPE meeting , pp.361-362, 2019

Aghayeva, A. Et Al. (2019) . "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency." 58th Annual ESPE meeting , pp.361-362.

@conferencepaper{conferencepaper, author={Asmar Aghayeva Et Al. }, title={Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency}, congress name={58th Annual ESPE meeting}, city={}, country={}, year={2019}, pages={361-362} }