Ozbek, M. N. Et Al. 2021. A rare and preventable aetiology of neurodevelopmental delay and epilepsy: familial glucocorticoid deficiency. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.34, no.11 , 1463-1468.

Ozbek, M. N., Demiral, M., Unal, E., Karasin, N. D., Baran, R. T., & DEMİRBİLEK, H., (2021). A rare and preventable aetiology of neurodevelopmental delay and epilepsy: familial glucocorticoid deficiency. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.34, no.11, 1463-1468.

Ozbek, Mehmet Et Al. "A rare and preventable aetiology of neurodevelopmental delay and epilepsy: familial glucocorticoid deficiency," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.34, no.11, 1463-1468, 2021

Ozbek, Mehmet N. Et Al. "A rare and preventable aetiology of neurodevelopmental delay and epilepsy: familial glucocorticoid deficiency." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.34, no.11, pp.1463-1468, 2021

Ozbek, M. N. Et Al. (2021) . "A rare and preventable aetiology of neurodevelopmental delay and epilepsy: familial glucocorticoid deficiency." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.34, no.11, pp.1463-1468.

@article{article, author={Mehmet Nuri Ozbek Et Al. }, title={A rare and preventable aetiology of neurodevelopmental delay and epilepsy: familial glucocorticoid deficiency}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2021, pages={1463-1468} }