2Ixunbroso S,Paris F,Sultan C. Activating Gsatpha mutations:analysis of 113 patients with signs of McCune,Albright 8y Tldmmea European col- laborative study. JClin Endoerinol Metab,2004,89(5) :2107-2113. 被引量:1
6Lumbroso S,Paris F,Sultan C.Activating Gsatpha mutations:Analysis of 113 patients with signs of McCune-Albright syndrome--A European collaborative study[J].J Clin Endocrinol Metab,2004,89(5):2107-2113. 被引量:1
7Idowu BD,Al-Adnani M,O'Donnell P,et al.A sensitive mutation-specific screening technique for GNAS1 mutations in cases of fibrous dysplasia:The first report of a codon 227 mutation in bone[J].Histopathology,2007,50(6):691-704. 被引量:1
8Collins M T,Shenker A.McCune-Albright Syndrome:New insight[J].Curr Opin Endocrinol Diabetes,1999,6(2):119-125. 被引量:1
9Marie PJ,de Pollak C,Chanson P,et al.Increased proliferation of osteoblastic cells expressing the activating Gs alpha mutation in monostotic and polyostotic fibrous dysplasia[J].Am J Pathol,1997,150(3):1059-1069. 被引量:1
10Ringel MD,Schwindinger WF,Levine MA.Clinical implications of genetic defects in G proteins.The molecular basis of McCuneAlbright syndrome and Albright hereditary osteodystrophy[J].Medicine,1996,75(4):171-184. 被引量:1