Aghayeva, A. Et Al. 2019. Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency. HORMONE RESEARCH IN PAEDIATRICS , vol.91 , 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. HORMONE RESEARCH IN PAEDIATRICS , vol.91, 361-362.

Aghayeva, Asmar Et Al. "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency," HORMONE RESEARCH IN PAEDIATRICS , vol.91, 361-362, 2019

Aghayeva, Asmar Et Al. "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency." HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.361-362, 2019

Aghayeva, A. Et Al. (2019) . "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency." HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.361-362.

@article{article, author={Asmar Aghayeva Et Al. }, title={Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2019, pages={361-362} }