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Journal Abstract Search

208 related items for PubMed ID: 8650126

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  • 2. Prenatal exclusion of Crouzon syndrome by mutation analysis of FGFR2.
    Phupong V, Srichomthong C, Shotelersuk V.
    Southeast Asian J Trop Med Public Health; 2004 Dec; 35(4):977-9. PubMed ID: 15916101
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  • 13. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes.
    Bellus GA, Gaudenz K, Zackai EH, Clarke LA, Szabo J, Francomano CA, Muenke M.
    Nat Genet; 1996 Oct; 14(2):174-6. PubMed ID: 8841188
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  • 14. A novel fibroblast growth factor receptor 2 mutation in Crouzon syndrome associated with Chiari type I malformation and syringomyelia.
    Fujisawa H, Hasegawa M, Kida S, Yamashita J.
    J Neurosurg; 2002 Aug; 97(2):396-400. PubMed ID: 12186468
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  • 16. [From gene to disease; craniosynostosis syndromes due to FGFR2-mutation].
    van Ravenswaaij-Arts CM, van den Ouweland AM, Hoogeboom AJ, Herbergs J, Pals G.
    Ned Tijdschr Geneeskd; 2002 Jan 12; 146(2):63-6. PubMed ID: 11820058
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  • 19. A novel FGFR2 gene mutation in Crouzon syndrome associated with apparent nonpenetrance.
    Everett ET, Britto DA, Ward RE, Hartsfield JK.
    Cleft Palate Craniofac J; 1999 Nov 12; 36(6):533-41. PubMed ID: 10574673
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