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, Birleşik Krallık, 28 - 31 Mayıs 2015, ss.430