Aghayeva , A. Et Al. 2019. Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency. 58th Annuel Meeting of the European Society for Paediatric Endocrinology /ESPE) , (Vienna, Austria), 361.

Aghayeva , A., Turan, H., Toksoy, G., Dagdeviren Cakir, A., Berkay, E., Güneş, N., ... Evliyaoğlu, S. O.(2019). Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency . 58th Annuel Meeting of the European Society for Paediatric Endocrinology /ESPE) (pp.361). Vienna, Austria

Aghayeva , Asmar Et Al. "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency," 58th Annuel Meeting of the European Society for Paediatric Endocrinology /ESPE), Vienna, Austria, 2019

Aghayeva , Asmar Et Al. "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency." 58th Annuel Meeting of the European Society for Paediatric Endocrinology /ESPE) , Vienna, Austria, pp.361, 2019

Aghayeva , A. Et Al. (2019) . "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency." 58th Annuel Meeting of the European Society for Paediatric Endocrinology /ESPE) , Vienna, Austria, p.361.

@conferencepaper{conferencepaper, author={Asmar Aghayeva Et Al. }, title={Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency}, congress name={58th Annuel Meeting of the European Society for Paediatric Endocrinology /ESPE)}, city={Vienna}, country={Austria}, year={2019}, pages={361} }