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650 related items for PubMed ID: 30251589

  • 1. Mutations in the ENG, ACVRL1, and SMAD4 genes and clinical manifestations of hereditary haemorrhagic telangiectasia: experience from the Center for Osler's Disease, Uppsala University Hospital.
    Karlsson T, Cherif H.
    Ups J Med Sci; 2018 Sep; 123(3):153-157. PubMed ID: 30251589
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  • 10. Genotype-phenotype correlation in hereditary hemorrhagic telangiectasia: mutations and manifestations.
    Bayrak-Toydemir P, McDonald J, Markewitz B, Lewin S, Miller F, Chou LS, Gedge F, Tang W, Coon H, Mao R.
    Am J Med Genet A; 2006 Mar 01; 140(5):463-70. PubMed ID: 16470787
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  • 13. Heart failure and pulmonary arteriovenous malformations in a patient with hereditary hemorrhagic telangiectasia type 2.
    Du J, Zhu Y, Zhang YL, Li S, Huang J, Luo XH, Liu L.
    J Thromb Thrombolysis; 2015 Nov 01; 40(4):515-9. PubMed ID: 26245826
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  • 14. Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network.
    Lesca G, Olivieri C, Burnichon N, Pagella F, Carette MF, Gilbert-Dussardier B, Goizet C, Roume J, Rabilloud M, Saurin JC, Cottin V, Honnorat J, Coulet F, Giraud S, Calender A, Danesino C, Buscarini E, Plauchu H, French-Italian-Rendu-Osler Network.
    Genet Med; 2007 Jan 01; 9(1):14-22. PubMed ID: 17224686
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