G. Öner Et Al. , "Infantile Hypercalcemia Type 2 Due to Novel Mutation in SLC34A1 Gene," 60th60.th Annual Meeting of the European Society for Paediatric Endocrinology , vol.95, no.2, Rome, Italy, pp.150, 2022
Öner, G. Et Al. 2022. Infantile Hypercalcemia Type 2 Due to Novel Mutation in SLC34A1 Gene. 60th60.th Annual Meeting of the European Society for Paediatric Endocrinology , (Rome, Italy), 150.
Öner, G., Döğer, E., Ceylaner, S., Kayhan, G., Bideci, A., & Çamurdan, M. O., (2022). Infantile Hypercalcemia Type 2 Due to Novel Mutation in SLC34A1 Gene . 60th60.th Annual Meeting of the European Society for Paediatric Endocrinology (pp.150). Rome, Italy
Öner, GANİMET Et Al. "Infantile Hypercalcemia Type 2 Due to Novel Mutation in SLC34A1 Gene," 60th60.th Annual Meeting of the European Society for Paediatric Endocrinology, Rome, Italy, 2022
Öner, GANİMET Et Al. "Infantile Hypercalcemia Type 2 Due to Novel Mutation in SLC34A1 Gene." 60th60.th Annual Meeting of the European Society for Paediatric Endocrinology , Rome, Italy, pp.150, 2022
Öner, G. Et Al. (2022) . "Infantile Hypercalcemia Type 2 Due to Novel Mutation in SLC34A1 Gene." 60th60.th Annual Meeting of the European Society for Paediatric Endocrinology , Rome, Italy, p.150.
@conferencepaper{conferencepaper, author={GANİMET ÖNER Et Al. }, title={Infantile Hypercalcemia Type 2 Due to Novel Mutation in SLC34A1 Gene}, congress name={60th60.th Annual Meeting of the European Society for Paediatric Endocrinology}, city={Rome}, country={Italy}, year={2022}, pages={150} }