G. YILDIZ Et Al. , "A RARE CAUSE OF COMBINED HEPATIC AND RENAL FAILURE: NPHP19 DUE TO A NOVEL DCDC2 VARIANT IN TWO SIBLINGS," PEDIATRIC NEPHROLOGY , vol.37, no.11, pp.2854-2855, 2022
YILDIZ, G. Et Al. 2022. A RARE CAUSE OF COMBINED HEPATIC AND RENAL FAILURE: NPHP19 DUE TO A NOVEL DCDC2 VARIANT IN TWO SIBLINGS. PEDIATRIC NEPHROLOGY , vol.37, no.11 , 2854-2855.
YILDIZ, G., TORUN BAYRAM, M., ÇAĞLAYAN, A. O., ÜLGENALP, A., SOYLU, A., & KAVUKÇU, S., (2022). A RARE CAUSE OF COMBINED HEPATIC AND RENAL FAILURE: NPHP19 DUE TO A NOVEL DCDC2 VARIANT IN TWO SIBLINGS. PEDIATRIC NEPHROLOGY , vol.37, no.11, 2854-2855.
YILDIZ, GİZEM Et Al. "A RARE CAUSE OF COMBINED HEPATIC AND RENAL FAILURE: NPHP19 DUE TO A NOVEL DCDC2 VARIANT IN TWO SIBLINGS," PEDIATRIC NEPHROLOGY , vol.37, no.11, 2854-2855, 2022
YILDIZ, GİZEM Et Al. "A RARE CAUSE OF COMBINED HEPATIC AND RENAL FAILURE: NPHP19 DUE TO A NOVEL DCDC2 VARIANT IN TWO SIBLINGS." PEDIATRIC NEPHROLOGY , vol.37, no.11, pp.2854-2855, 2022
YILDIZ, G. Et Al. (2022) . "A RARE CAUSE OF COMBINED HEPATIC AND RENAL FAILURE: NPHP19 DUE TO A NOVEL DCDC2 VARIANT IN TWO SIBLINGS." PEDIATRIC NEPHROLOGY , vol.37, no.11, pp.2854-2855.
@article{article, author={GİZEM YILDIZ Et Al. }, title={A RARE CAUSE OF COMBINED HEPATIC AND RENAL FAILURE: NPHP19 DUE TO A NOVEL DCDC2 VARIANT IN TWO SIBLINGS}, journal={PEDIATRIC NEPHROLOGY}, year=2022, pages={2854-2855} }