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Journal Abstract Search

310 related items for PubMed ID: 11711827

  • 21.
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  • 22. Molecular diagnosis of Apert syndrome in Chinese patients.
    Tsai FJ, Tsai CH, Peng CT, Lin SP, Hwu WL, Wang TR, Lee CC, Wu JY.
    Acta Paediatr Taiwan; 1999; 40(1):31-3. PubMed ID: 10910582
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  • 24. Re: Sequence analysis of fibroblast growth factor receptor 2 (FGFR2) in Japanese patients with craniosynostosis. Sakai et al. J Craniofac. Surg. 2001, 12: 580-585.
    Warren SM, Longaker MT.
    J Craniofac Surg; 2002 Jul; 13(4):597-9. PubMed ID: 12140430
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  • 25. Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses).
    Kress W, Collmann H, Büsse M, Halliger-Keller B, Mueller CR.
    Cytogenet Cell Genet; 2000 Jul; 91(1-4):134-7. PubMed ID: 11173845
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  • 26. Mutation detection in FGFR2 craniosynostosis syndromes.
    Hollway GE, Suthers GK, Haan EA, Thompson E, David DJ, Gecz J, Mulley JC.
    Hum Genet; 1997 Feb; 99(2):251-5. PubMed ID: 9048930
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  • 29. Expression profiles of craniosynostosis-derived fibroblasts.
    Carinci F, Bodo M, Tosi L, Francioso F, Evangelisti R, Pezzetti F, Scapoli L, Martinelli M, Baroni T, Stabellini G, Carinci P, Bellucci C, Lilli C, Volinia S.
    Mol Med; 2002 Oct; 8(10):638-44. PubMed ID: 12477974
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  • 30. Novel mutation in the FGFR2 gene at the same codon as the Crouzon syndrome mutations in a severe Pfeiffer syndrome type 2 case.
    Schaefer F, Anderson C, Can B, Say B.
    Am J Med Genet; 1998 Jan 23; 75(3):252-5. PubMed ID: 9475591
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  • 33. Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome.
    Oldridge M, Wilkie AO, Slaney SF, Poole MD, Pulleyn LJ, Rutland P, Hockley AD, Wake MJ, Goldin JH, Winter RM.
    Hum Mol Genet; 1995 Jun 23; 4(6):1077-82. PubMed ID: 7655462
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