Kisla, E. Et Al. 2020. Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?. CEN case reports , vol.9, no.4 , 344-346.

Kisla, E., Altun, İ., Bisgin, A., Atmis, B., Altintas, D., & Balcı, S., (2020). Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?. CEN case reports , vol.9, no.4, 344-346.

Kisla, RABİA Et Al. "Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?," CEN case reports , vol.9, no.4, 344-346, 2020

Kisla, RABİA M. Et Al. "Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?." CEN case reports , vol.9, no.4, pp.344-346, 2020

Kisla, E. Et Al. (2020) . "Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?." CEN case reports , vol.9, no.4, pp.344-346.

@article{article, author={RABİA MİRAY KIŞLA EKİNCİ Et Al. }, title={Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?}, journal={CEN case reports}, year=2020, pages={344-346} }