ÖZSU CAVGA, E. Et Al. 2019. Typical phenotype of isolated aldosterone synthetase (AS) deficiency in two infants with heterozygous AS gene mutation: Dilemma for diagnosis. HORMONE RESEARCH IN PAEDIATRICS , vol.91 , 504-505.

ÖZSU CAVGA, E., CERAN, A., Uyanik, R., Bilici, E., Cetin, T., ŞIKLAR, Z., ... AYCAN, Z.(2019). Typical phenotype of isolated aldosterone synthetase (AS) deficiency in two infants with heterozygous AS gene mutation: Dilemma for diagnosis. HORMONE RESEARCH IN PAEDIATRICS , vol.91, 504-505.

ÖZSU CAVGA, ELİF Et Al. "Typical phenotype of isolated aldosterone synthetase (AS) deficiency in two infants with heterozygous AS gene mutation: Dilemma for diagnosis," HORMONE RESEARCH IN PAEDIATRICS , vol.91, 504-505, 2019

ÖZSU CAVGA, ELİF Et Al. "Typical phenotype of isolated aldosterone synthetase (AS) deficiency in two infants with heterozygous AS gene mutation: Dilemma for diagnosis." HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.504-505, 2019

ÖZSU CAVGA, E. Et Al. (2019) . "Typical phenotype of isolated aldosterone synthetase (AS) deficiency in two infants with heterozygous AS gene mutation: Dilemma for diagnosis." HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.504-505.

@article{article, author={ELİF ÖZSU Et Al. }, title={Typical phenotype of isolated aldosterone synthetase (AS) deficiency in two infants with heterozygous AS gene mutation: Dilemma for diagnosis}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2019, pages={504-505} }