Y. Sağlıker Et Al. , "Novel striking mismutations on GNAS1, FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination-compulsion of bone displasias-hereditary osteodystrophies and CKD. 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. 28 - 31 May 2015 / UK, London, Free communication.," 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. , Londra, United Kingdom, pp.432, 2015
Sağlıker, Y. Et Al. 2015. Novel striking mismutations on GNAS1, FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination-compulsion of bone displasias-hereditary osteodystrophies and CKD. 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. 28 - 31 May 2015 / UK, London, Free communication.. 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. , (Londra, United Kingdom), 432.
Sağlıker, Y., DEMİRHAN, O., & ark., v., (2015). Novel striking mismutations on GNAS1, FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination-compulsion of bone displasias-hereditary osteodystrophies and CKD. 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. 28 - 31 May 2015 / UK, London, Free communication. . 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. (pp.432). Londra, United Kingdom
Sağlıker, Yahya, OSMAN DEMİRHAN, And ve ark.. "Novel striking mismutations on GNAS1, FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination-compulsion of bone displasias-hereditary osteodystrophies and CKD. 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. 28 - 31 May 2015 / UK, London, Free communication.," 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress., Londra, United Kingdom, 2015
Sağlıker, Yahya Et Al. "Novel striking mismutations on GNAS1, FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination-compulsion of bone displasias-hereditary osteodystrophies and CKD. 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. 28 - 31 May 2015 / UK, London, Free communication.." 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. , Londra, United Kingdom, pp.432, 2015
Sağlıker, Y. DEMİRHAN, O. And ark., v. (2015) . "Novel striking mismutations on GNAS1, FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination-compulsion of bone displasias-hereditary osteodystrophies and CKD. 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. 28 - 31 May 2015 / UK, London, Free communication.." 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. , Londra, United Kingdom, p.432.
@conferencepaper{conferencepaper, author={Yahya Sağlıker Et Al. }, title={Novel striking mismutations on GNAS1, FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination-compulsion of bone displasias-hereditary osteodystrophies and CKD. 52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress. 28 - 31 May 2015 / UK, London, Free communication.}, congress name={52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress.}, city={Londra}, country={United Kingdom}, year={2015}, pages={432} }