ÇAĞAN, M. Et Al. 2021. Obstetrical history of a family with combined oxidative phosphorylation deficiency 3 and methylenetetrahydrofolate reductase polymorphisms. CASE REPORTS IN PERINATAL MEDICINE , vol.10, no.1 .

ÇAĞAN, M., ÜNAL, C., ÜREL DEMİR, G., FADILOĞLU, E., ÖZGÜL, R. K., & Belcsac, M. S., (2021). Obstetrical history of a family with combined oxidative phosphorylation deficiency 3 and methylenetetrahydrofolate reductase polymorphisms. CASE REPORTS IN PERINATAL MEDICINE , vol.10, no.1.

ÇAĞAN, MURAT Et Al. "Obstetrical history of a family with combined oxidative phosphorylation deficiency 3 and methylenetetrahydrofolate reductase polymorphisms," CASE REPORTS IN PERINATAL MEDICINE , vol.10, no.1, 2021

ÇAĞAN, MURAT Et Al. "Obstetrical history of a family with combined oxidative phosphorylation deficiency 3 and methylenetetrahydrofolate reductase polymorphisms." CASE REPORTS IN PERINATAL MEDICINE , vol.10, no.1, 2021

ÇAĞAN, M. Et Al. (2021) . "Obstetrical history of a family with combined oxidative phosphorylation deficiency 3 and methylenetetrahydrofolate reductase polymorphisms." CASE REPORTS IN PERINATAL MEDICINE , vol.10, no.1.

@article{article, author={MURAT ÇAĞAN Et Al. }, title={Obstetrical history of a family with combined oxidative phosphorylation deficiency 3 and methylenetetrahydrofolate reductase polymorphisms}, journal={CASE REPORTS IN PERINATAL MEDICINE}, year=2021}