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Page 1
A gene for FG syndrome maps in the Xq12-q21.31 region.
Briault S, Hill R, Shrimpton A, Zhu D, Till M, Ronce N, Margaritte-Jeannin P, Baraitser M, Middleton-Price H, Malcolm S, Thompson E, Hoo J, Wilson G, Romano C, Guichet A, Pembrey M, Fontes M, Poustka A, Moraine C. Briault S, et al. Among authors: pembrey m. Am J Med Genet. 1997 Nov 28;73(1):87-90. Am J Med Genet. 1997. PMID: 9375929
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. Briault S, et al. Among authors: pembrey m. Am J Med Genet. 2000 Nov 13;95(2):178-81. doi: 10.1002/1096-8628(20001113)95:2<178::aid-ajmg17>3.0.co;2-v. Am J Med Genet. 2000. PMID: 11078572
Seckel syndrome: an overdiagnosed syndrome.
Thompson E, Pembrey M. Thompson E, et al. Among authors: pembrey m. J Med Genet. 1985 Jun;22(3):192-201. doi: 10.1136/jmg.22.3.192. J Med Genet. 1985. PMID: 4040172 Free PMC article.
Phenotypic variation in LADD syndrome.
Thompson E, Pembrey M, Graham JM. Thompson E, et al. Among authors: pembrey m. J Med Genet. 1985 Oct;22(5):382-5. doi: 10.1136/jmg.22.5.382. J Med Genet. 1985. PMID: 4078868 Free PMC article.
Trigonocephaly and the Opitz C syndrome.
Sargent C, Burn J, Baraitser M, Pembrey ME. Sargent C, et al. Among authors: pembrey me. J Med Genet. 1985 Feb;22(1):39-45. doi: 10.1136/jmg.22.1.39. J Med Genet. 1985. PMID: 3981579 Free PMC article.
261 results