O. DEMİRHAN Et Al. , "Whole 13 exons of GNAS1 gene ın saglıker syndrome (SS). combınatıon-compulsıon of bone dysplasıas-heredıtary osteodıstrophıes (BD), chronıc kıdney dıseases (CKD) and secondary hyperparathyroıdısm.," 52nd European Renal Association - European Dialysis and Transplant Association (ERA-EDTA) Congress. , Londra, United Kingdom, pp.430, 2015
DEMİRHAN, O. Et Al. 2015. Whole 13 exons of GNAS1 gene ın saglıker syndrome (SS). combınatıon-compulsıon of bone dysplasıas-heredıtary osteodıstrophıes (BD), chronıc kıdney dıseases (CKD) and secondary hyperparathyroıdısm.. 52nd European Renal Association - European Dialysis and Transplant Association (ERA-EDTA) Congress. , (Londra, United Kingdom), 430.
DEMİRHAN, O., Sağlıker, Y., & ark., v., (2015). Whole 13 exons of GNAS1 gene ın saglıker syndrome (SS). combınatıon-compulsıon of bone dysplasıas-heredıtary osteodıstrophıes (BD), chronıc kıdney dıseases (CKD) and secondary hyperparathyroıdısm. . 52nd European Renal Association - European Dialysis and Transplant Association (ERA-EDTA) Congress. (pp.430). Londra, United Kingdom
DEMİRHAN, OSMAN, Yahya Sağlıker, And ve ark.. "Whole 13 exons of GNAS1 gene ın saglıker syndrome (SS). combınatıon-compulsıon of bone dysplasıas-heredıtary osteodıstrophıes (BD), chronıc kıdney dıseases (CKD) and secondary hyperparathyroıdısm.," 52nd European Renal Association - European Dialysis and Transplant Association (ERA-EDTA) Congress., Londra, United Kingdom, 2015
DEMİRHAN, OSMAN Et Al. "Whole 13 exons of GNAS1 gene ın saglıker syndrome (SS). combınatıon-compulsıon of bone dysplasıas-heredıtary osteodıstrophıes (BD), chronıc kıdney dıseases (CKD) and secondary hyperparathyroıdısm.." 52nd European Renal Association - European Dialysis and Transplant Association (ERA-EDTA) Congress. , Londra, United Kingdom, pp.430, 2015
DEMİRHAN, O. Sağlıker, Y. And ark., v. (2015) . "Whole 13 exons of GNAS1 gene ın saglıker syndrome (SS). combınatıon-compulsıon of bone dysplasıas-heredıtary osteodıstrophıes (BD), chronıc kıdney dıseases (CKD) and secondary hyperparathyroıdısm.." 52nd European Renal Association - European Dialysis and Transplant Association (ERA-EDTA) Congress. , Londra, United Kingdom, p.430.
@conferencepaper{conferencepaper, author={OSMAN DEMİRHAN Et Al. }, title={Whole 13 exons of GNAS1 gene ın saglıker syndrome (SS). combınatıon-compulsıon of bone dysplasıas-heredıtary osteodıstrophıes (BD), chronıc kıdney dıseases (CKD) and secondary hyperparathyroıdısm.}, congress name={52nd European Renal Association - European Dialysis and Transplant Association (ERA-EDTA) Congress.}, city={Londra}, country={United Kingdom}, year={2015}, pages={430} }