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Journal Abstract Search


478 related items for PubMed ID: 26289989

  • 1. Clinical and genetic characteristics of craniosynostosis in Hungary.
    Bessenyei B, Nagy A, Szakszon K, Mokánszki A, Balogh E, Ujfalusi A, Tihanyi M, Novák L, Bognár L, Oláh É.
    Am J Med Genet A; 2015 Dec; 167A(12):2985-91. PubMed ID: 26289989
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  • 3. Somatic FGFR and TWIST mutations are not a common cause of isolated nonsyndromic single suture craniosynostosis.
    Anderson PJ, Cox TC, Roscioli T, Elakis G, Smithers L, David DJ, Powell B.
    J Craniofac Surg; 2007 Mar; 18(2):312-4. PubMed ID: 17414280
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  • 6. 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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  • 9. Germline mutation screening of the Saethre-Chotzen-associated genes TWIST1 and FGFR3 in families with BRCA1/2-negative breast cancer.
    Bergman A, Sahlin P, Emanuelsson M, Carén H, Tarnow P, Martinsson T, Grönberg H, Stenman G.
    Scand J Plast Reconstr Surg Hand Surg; 2009 May; 43(5):251-5. PubMed ID: 19863427
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  • 10. Clinical study and some molecular features of Mexican patients with syndromic craniosynostosis.
    Ibarra-Arce A, Almaraz-Salinas M, Martínez-Rosas V, Ortiz de Zárate-Alarcón G, Flores-Peña L, Romero-Valdovinos M, Olivo-Díaz A.
    Mol Genet Genomic Med; 2020 Aug; 8(8):e1266. PubMed ID: 32510873
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  • 12. Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.
    Ye X, Guilmatre A, Reva B, Peter I, Heuzé Y, Richtsmeier JT, Fox DJ, Goedken RJ, Jabs EW, Romitti PA.
    Plast Reconstr Surg; 2016 Mar; 137(3):952-961. PubMed ID: 26910679
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  • 14. Molecular and cellular bases of syndromic craniosynostoses.
    Bonaventure J, El Ghouzzi V.
    Expert Rev Mol Med; 2003 Jan 29; 5(4):1-17. PubMed ID: 14987407
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  • 16. [Clinical and genetic characteristics of craniosynostosis].
    Bessenyei B, Oláh E.
    Orv Hetil; 2014 Mar 02; 155(9):341-7. PubMed ID: 24566698
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  • 19. Mutation analysis of FGFR1-3 in 11 Japanese patients with syndromic craniosynostoses.
    Ohishi A, Nishimura G, Kato F, Ono H, Maruwaka K, Ago M, Suzumura H, Hirose E, Uchida Y, Fukami M, Ogata T.
    Am J Med Genet A; 2017 Jan 02; 173(1):157-162. PubMed ID: 27683237
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  • 20. Craniosynostosis and related limb anomalies.
    Wilkie AO, Oldridge M, Tang Z, Maxson RE.
    Novartis Found Symp; 2001 Jan 02; 232():122-33; discussion 133-43. PubMed ID: 11277076
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