Tekkeşin, F. Et Al. 2022. Endothelial nitric oxide synthase G894T, intron 4 VNTR, and T786C polymorphisms in retinopathy of prematurity. Journal of Neonatal-Perinatal Medicine , vol.15, no.2 , 249-255.

Tekkeşin, F., Yurdakok, M., GÜMÜŞ, E., BABAOĞLU, M. Ö., Bozkurt, A., Caliskan Kadayifcilar, S., ... Eldem, M.(2022). Endothelial nitric oxide synthase G894T, intron 4 VNTR, and T786C polymorphisms in retinopathy of prematurity. Journal of Neonatal-Perinatal Medicine , vol.15, no.2, 249-255.

Tekkeşin, F. Et Al. "Endothelial nitric oxide synthase G894T, intron 4 VNTR, and T786C polymorphisms in retinopathy of prematurity," Journal of Neonatal-Perinatal Medicine , vol.15, no.2, 249-255, 2022

Tekkeşin, F. Et Al. "Endothelial nitric oxide synthase G894T, intron 4 VNTR, and T786C polymorphisms in retinopathy of prematurity." Journal of Neonatal-Perinatal Medicine , vol.15, no.2, pp.249-255, 2022

Tekkeşin, F. Et Al. (2022) . "Endothelial nitric oxide synthase G894T, intron 4 VNTR, and T786C polymorphisms in retinopathy of prematurity." Journal of Neonatal-Perinatal Medicine , vol.15, no.2, pp.249-255.

@article{article, author={F. Tekkeşin Et Al. }, title={Endothelial nitric oxide synthase G894T, intron 4 VNTR, and T786C polymorphisms in retinopathy of prematurity}, journal={Journal of Neonatal-Perinatal Medicine}, year=2022, pages={249-255} }