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4,205 results

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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: thompson e. Am J Med Genet. 1997 Nov 28;73(1):87-90. Am J Med Genet. 1997. PMID: 9375929
FG syndrome.
Thompson E, Baraitser M. Thompson E, et al. J Med Genet. 1987 Mar;24(3):139-43. doi: 10.1136/jmg.24.3.139. J Med Genet. 1987. PMID: 3572995 Free PMC article. No abstract available.
Seckel syndrome: an overdiagnosed syndrome.
Thompson E, Pembrey M. Thompson E, et al. 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. 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.
Severe Silver-Russell syndrome.
Donnai D, Thompson E, Allanson J, Baraitser M. Donnai D, et al. Among authors: thompson e. J Med Genet. 1989 Jul;26(7):447-51. doi: 10.1136/jmg.26.7.447. J Med Genet. 1989. PMID: 2746617 Free PMC article.
Nosology of Smith-Lemli-Opitz syndrome.
Thompson E, Baraitser M. Thompson E, et al. Am J Med Genet. 1987 Nov;28(3):733-4. doi: 10.1002/ajmg.1320280321. Am J Med Genet. 1987. PMID: 3322012 Review. No abstract available.
4,205 results