Karakilic-Ozturan, E. Et Al. 2022. SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS. ACTA ENDOCRINOLOGICA-BUCHAREST , vol.18, no.3 , 387-391.

Karakilic-Ozturan, E., ÖZTÜRK, A., ÖNEY, C., KARDELEN AL, A. D., YÜRÜK YILDIRIM, Z. N., BALCI, H. İ., ... POYRAZOĞLU, Ş.(2022). SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS. ACTA ENDOCRINOLOGICA-BUCHAREST , vol.18, no.3, 387-391.

Karakilic-Ozturan, Esin Et Al. "SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS," ACTA ENDOCRINOLOGICA-BUCHAREST , vol.18, no.3, 387-391, 2022

Karakilic-Ozturan, Esin K. Et Al. "SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS." ACTA ENDOCRINOLOGICA-BUCHAREST , vol.18, no.3, pp.387-391, 2022

Karakilic-Ozturan, E. Et Al. (2022) . "SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS." ACTA ENDOCRINOLOGICA-BUCHAREST , vol.18, no.3, pp.387-391.

@article{article, author={Esin KARAKILIÇ ÖZTURAN Et Al. }, title={SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS}, journal={ACTA ENDOCRINOLOGICA-BUCHAREST}, year=2022, pages={387-391} }