7 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 33512531 | Genotype-Phenotype Correlation in Fibrous Dysplasia/McCune-Albright Syndrome. | 2021 Apr 23 | 1 |
2 | 17873334 | Genetic diagnosis of multiple affected tissues in a patient with McCune-Albright syndrome. | 2007 Apr | 1 |
3 | 15368366 | Mutation of the highly conserved Arg165 and Glu168 residues of human Gsalpha disrupts the alphaD-alphaE loop and enhances basal GDP/GTP exchange rate. | 2004 Oct 1 | 2 |
4 | 12727968 | Cushing's syndrome secondary to adrenocorticotropin-independent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene. | 2003 May | 1 |
5 | 12374458 | A novel, complex heterozygous mutation within Gsalpha gene in patient with McCune-Albright syndrome. | 2002 Jul | 2 |
6 | 11272890 | A comparative study of fibrous dysplasia and osteofibrous dysplasia with regard to Gsalpha mutation at the Arg201 codon: polymerase chain reaction-restriction fragment length polymorphism analysis of paraffin-embedded tissues. | 2000 May | 1 |
7 | 8126161 | An unusual presentation of McCune-Albright syndrome confirmed by an activating mutation of the Gs alpha-subunit from a bone lesion. | 1994 Mar | 3 |