Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.

Author:

McAllister K A,Lennon F,Bowles-Biesecker B,McKinnon W C,Helmbold E A,Markel D S,Jackson C E,Guttmacher A E,Pericak-Vance M A,Marchuk D A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. Neurological manifestations of hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): report of two cases and review of the literature;Roman, G.; Fisher, M.; Perl, D.; Poser, C.;Ann Neurol,1978

2. Hereditary haemorrhagic telangiectasia: a clinical analysis;Porteous, M.E.M.; Bum, J.; Proctor, S.;J Med Genet,1992

3. Clinical manifestations of hereditary hemorrhagic telangiectasia;Reilly, P.J.; Nostrant, T.T.,1984

4. Clinical spectrum of hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease);Peery, W.H.;Am _7 Med,1987

5. Agerelated clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population;Plauchu, H.; Chadarevian, J.-P.; Bideau, A.; Robert, J.-M.;Am JMed Genet,1989

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