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Journal Abstract Search

209 related items for PubMed ID: 10712195

  • 21. Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans.
    Meyers GA, Orlow SJ, Munro IR, Przylepa KA, Jabs EW.
    Nat Genet; 1995 Dec; 11(4):462-4. PubMed ID: 7493034
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  • 24. 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; 36(6):533-41. PubMed ID: 10574673
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  • 26. Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review.
    Nur BG, Pehlivanoğlu S, Mıhçı E, Calışkan M, Demir D, Alper OM, Kayserili H, Lüleci G.
    Pediatr Neurol; 2014 May; 50(5):482-90. PubMed ID: 24656465
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  • 27. Molecular diagnosis of bilateral coronal synostosis.
    Mulliken JB, Steinberger D, Kunze S, Müller U.
    Plast Reconstr Surg; 1999 Nov; 104(6):1603-15. PubMed ID: 10541159
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  • 28. Mutation of the fibroblast growth factor receptor 2 gene in Japanese patients with Apert syndrome.
    Matsumoto K, Urano Y, Kubo Y, Nakanishi H, Arase S.
    Plast Reconstr Surg; 1998 Feb; 101(2):307-11. PubMed ID: 9462761
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  • 35. A case of Pfeiffer syndrome type 1 with an A344P mutation in the FGFR2 gene.
    Shotelersuk V, Srivuthana S, Ittiwut C, Theamboonlers A, Mahatumarat C, Poovorawan Y.
    Southeast Asian J Trop Med Public Health; 2001 Jun; 32(2):425-8. PubMed ID: 11556600
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  • 38. Pfeiffer syndrome caused by haploinsufficient mutation of FGFR2.
    Tsukuno M, Suzuki H, Eto Y.
    J Craniofac Genet Dev Biol; 1999 Jun; 19(4):183-8. PubMed ID: 10731087
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