Kara, O. Et Al. 2021. A Novel Homozygous Mutation in CYP11A1 Gene is Associated with Severe Adrenal Insufficiency in 46, XX Patient. FETAL AND PEDIATRIC PATHOLOGY , vol.40, no.5 , 518-522.

Kara, O., Gorukmez, O., Ekici, A., & ÇELİK, F., (2021). A Novel Homozygous Mutation in CYP11A1 Gene is Associated with Severe Adrenal Insufficiency in 46, XX Patient. FETAL AND PEDIATRIC PATHOLOGY , vol.40, no.5, 518-522.

Kara, Ozlem Et Al. "A Novel Homozygous Mutation in CYP11A1 Gene is Associated with Severe Adrenal Insufficiency in 46, XX Patient," FETAL AND PEDIATRIC PATHOLOGY , vol.40, no.5, 518-522, 2021

Kara, Ozlem Et Al. "A Novel Homozygous Mutation in CYP11A1 Gene is Associated with Severe Adrenal Insufficiency in 46, XX Patient." FETAL AND PEDIATRIC PATHOLOGY , vol.40, no.5, pp.518-522, 2021

Kara, O. Et Al. (2021) . "A Novel Homozygous Mutation in CYP11A1 Gene is Associated with Severe Adrenal Insufficiency in 46, XX Patient." FETAL AND PEDIATRIC PATHOLOGY , vol.40, no.5, pp.518-522.

@article{article, author={Ozlem Kara Et Al. }, title={A Novel Homozygous Mutation in CYP11A1 Gene is Associated with Severe Adrenal Insufficiency in 46, XX Patient}, journal={FETAL AND PEDIATRIC PATHOLOGY}, year=2021, pages={518-522} }