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Journal Abstract Search

508 related items for PubMed ID: 9263339

  • 1. Ascending aortic aneurysm with or without features of Marfan syndrome and other fibrillinopathies: new insights.
    Furthmayr H, Francke U.
    Semin Thorac Cardiovasc Surg; 1997 Jul; 9(3):191-205. PubMed ID: 9263339
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  • 3. The molecular genetics of Marfan syndrome and related microfibrillopathies.
    Robinson PN, Godfrey M.
    J Med Genet; 2000 Jan; 37(1):9-25. PubMed ID: 10633129
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  • 5. Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome.
    Loeys B, Nuytinck L, Delvaux I, De Bie S, De Paepe A.
    Arch Intern Med; 2001 Nov 12; 161(20):2447-54. PubMed ID: 11700157
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  • 7. Orofacial manifestations of congenital fibrillin deficiency: pathogenesis and clinical diagnostics.
    De Coster PJ, Martens LC, De Paepe A.
    Pediatr Dent; 2004 Nov 12; 26(6):535-7. PubMed ID: 15646918
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  • 8. Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome.
    Pereira L, Andrikopoulos K, Tian J, Lee SY, Keene DR, Ono R, Reinhardt DP, Sakai LY, Biery NJ, Bunton T, Dietz HC, Ramirez F.
    Nat Genet; 1997 Oct 12; 17(2):218-22. PubMed ID: 9326947
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  • 10. Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations.
    Faivre L, Masurel-Paulet A, Collod-Béroud G, Callewaert BL, Child AH, Stheneur C, Binquet C, Gautier E, Chevallier B, Huet F, Loeys BL, Arbustini E, Mayer K, Arslan-Kirchner M, Kiotsekoglou A, Comeglio P, Grasso M, Halliday DJ, Béroud C, Bonithon-Kopp C, Claustres M, Robinson PN, Adès L, De Backer J, Coucke P, Francke U, De Paepe A, Boileau C, Jondeau G.
    Pediatrics; 2009 Jan 12; 123(1):391-8. PubMed ID: 19117906
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  • 11. Clinical, pathological and molecular genetic findings in a case of neonatal Marfan syndrome.
    Bresters D, Nikkels PG, Meijboom EJ, Hoorntje TM, Pals G, Beemer FA.
    Acta Paediatr; 1999 Jan 12; 88(1):98-101. PubMed ID: 10090557
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  • 12. The molecular pathogenesis of the Marfan syndrome.
    Robinson PN, Booms P.
    Cell Mol Life Sci; 2001 Oct 12; 58(11):1698-707. PubMed ID: 11706995
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  • 13. Clinical and genetic associations in Marfan syndrome and related disorders.
    Ramirez F, Lee B, Vitale E.
    Mt Sinai J Med; 1992 Sep 12; 59(4):350-6. PubMed ID: 1406753
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  • 14. Two novel fibrillin-2 mutations in congenital contractural arachnodactyly.
    Belleh S, Zhou G, Wang M, Der Kaloustian VM, Pagon RA, Godfrey M.
    Am J Med Genet; 2000 May 01; 92(1):7-12. PubMed ID: 10797416
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