ÖZDEMİR, A. Et Al. 2018. Two Neonatal 21-Hydroxylase Deficiency Cases withoutHyperpigmentation. Annals of Clinical Case Reports , vol.3, no.1544 , 1-3.

ÖZDEMİR, A., KURTOĞLU, S., GÜL ŞİRAZ, Ü., HATİPOĞLU, N., & GÜNEŞ, T., (2018). Two Neonatal 21-Hydroxylase Deficiency Cases withoutHyperpigmentation. Annals of Clinical Case Reports , vol.3, no.1544, 1-3.

ÖZDEMİR, AHMET Et Al. "Two Neonatal 21-Hydroxylase Deficiency Cases withoutHyperpigmentation," Annals of Clinical Case Reports , vol.3, no.1544, 1-3, 2018

ÖZDEMİR, AHMET Et Al. "Two Neonatal 21-Hydroxylase Deficiency Cases withoutHyperpigmentation." Annals of Clinical Case Reports , vol.3, no.1544, pp.1-3, 2018

ÖZDEMİR, A. Et Al. (2018) . "Two Neonatal 21-Hydroxylase Deficiency Cases withoutHyperpigmentation." Annals of Clinical Case Reports , vol.3, no.1544, pp.1-3.

@article{article, author={AHMET ÖZDEMİR Et Al. }, title={Two Neonatal 21-Hydroxylase Deficiency Cases withoutHyperpigmentation}, journal={Annals of Clinical Case Reports}, year=2018, pages={1-3} }