AGHAYEVA, A. Et Al. 2019. Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency. Annual ESPE Meeting 2019 , (Austria).

AGHAYEVA, A., TURAN, H., TOKSOY, G., DAĞDEVİREN ÇAKIR, A., BERKAY, E. G., GÜNEŞ, N., ... EVLİYAOĞLU, S. O.(2019). Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency . Annual ESPE Meeting 2019, Austria

AGHAYEVA, ASMAR Et Al. "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency," Annual ESPE Meeting 2019, Austria, 2019

AGHAYEVA, ASMAR Et Al. "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency." Annual ESPE Meeting 2019 , Austria, 2019

AGHAYEVA, A. Et Al. (2019) . "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency." Annual ESPE Meeting 2019 , Austria.

@conferencepaper{conferencepaper, author={ASMAR AGHAYEVA Et Al. }, title={Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency}, congress name={Annual ESPE Meeting 2019}, city={}, country={Austria}, year={2019}}