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A Rare Case of Upper Gastrointestinal Bleeding: Osler-Weber-Rendu Syndrome
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Table e-3: Genetic data of A-T patients with mild phenotypes from the Dutch cohort and literature.
Table e-1: Clinical and laboratory data of 105 A-T patients with mild phenotypes from the Dutch cohort and literature.
Current Status of Clinical and Genetic Screening of Hereditary Hemorrhagic Telangiectasia Families in Hungary
Polymorphisms in ACVRL1 and Endoglin Genes are Not Associated with Sporadic and HHT-Related Brain AVMs in Dutch Patients