Citations for
1FLNA, 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
2FGS1, 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
3FGS1, 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