| 1 | MCAS, GNAS
|
| Genetics of McCune-Albright syndrome.
|
| de Sanctis L, Delmastro L, Russo MC, Matarazzo P, Lala R, de Sanctis C.
|
| J Pediatr Endocrinol Metab 19 Suppl 2:577-82. Review. 2006
|
| 2 | GNAS, MCAS
|
| Activating Gsalpha mutations: analysis of 113 patients with signs of McCune-Albright syndrome--a European Collaborative Study.
|
| Lumbroso S, Paris F, Sultan C; European Collaborative Study.
|
| J Clin Endocrinol Metab 89(5):2107-13.
2004
|
| 3 | GNAS, MCAS
|
| Thyroid carcinoma in the McCune-Albright syndrome: contributory role of activating Gs alpha mutations.
|
| Collins MT, Sarlis NJ, Merino MJ, Monroe J, Crawford SE, Krakoff JA, Guthrie LC, Bonat S, Robey PG, Shenker A.
|
| J Clin Endocrinol Metab 88(9):4413-7.
2003
|
| 4 | GNAS, MCAS
|
| Fibrous dysplasia is a neoplasm.
|
| Cohen MM Jr.
|
| Am J Med Genet 98(4):290-3. No abstract available. 2001
|
| 5 | GNAS, MCAS
|
| Mutations of the GNAS1 gene, stromal cell dysfunction, and osteomalacic changes in non-McCune-Albright fibrous dysplasia of bone.
|
| Bianco P, Riminucci M, Majolagbe A, Kuznetsov SA, Collins MT, Mankani MH, Corsi A, Bone HG, Wientroub S, Spiegel AM, Fisher LW, Robey PG.
|
| J Bone Miner Res 15(1):120-8. 2000
|
| 6 | GNAS, MCAS
|
| Demonstration of McCune-Albright mutations in the liver of children with high gammaGT progressive cholestasis.
|
| Silva ES, Lumbroso S, Medina M, Gillerot Y, Sultan C, Sokal EM.
|
| J Hepatol 32(1):154-8. 2000
|
| 7 | MCAS, GNAS
|
| Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein Gs.
|
| Shenker A, et al.
|
| J Pediatr 123 : 509-518. 1993
|