| 1 | FLNA, FGS2 |
| Filamin A mutation is one cause of FG syndrome. | |
| Unger S, Mainberger A, Spitz C, Bahr A, Zeschnigk C, Zabel B, Superti-Furga A, Morris-Rosendahl DJ. | |
| Am J Med Genet A 143(16):1876-9. 2007 | |
| 2 | FGS1, FGS2, FGS3 |
| FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]. | |
| Dessay S, Moizard MP, Gilardi JL, Opitz JM, Middleton-Price H, Pembrey M, Moraine C, Briault S. | |
| Am J Med Genet 112(1):6-11. Review. 2002 | |
| 3 | FGS1, FGS2 |
| Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: A second FG locus [FGS2]? | |
| Briault S, Villard L, Rogner U, Coy J, Odent S, Lucas J, Passage E, Zhu D, Shrimpton A, Pembrey M, Till M, Guichet A, Dessay S, Fontes M, Poustka A, Moraine C. | |
| Am J Med Genet 95(2):178-181. 2000 | |