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- Letteboer, T G W [remove] 2
- 616.042 2
- Medical genetics -- Periodicals 2
- ALK1, activin receptor-like kinase 1 -- AVM, arteriovenous malformation -- ENG, endoglin -- GI, gastrointestinal -- JP, juvenile polyposis -- TGF, transforming growth factor 1
- CAVM, cerebral arteriovenous malformation -- CT, computed tomography -- GI, gastrointestinal -- HAVM, hepatic arteriovenous malformation -- HHT, hereditary haemorrhagic telangiectasia -- MRI, magnetic resonance imaging -- PAVM, pulmonary arteriovenous malformation 1
- hereditary haemorrhagic telangiectasia (HHT) -- juvenile polyposis (JP) -- endoglin (ENG) -- activin receptor-like kinase 1 (ALK1, ACVRL1) -- SMAD4 1
- hereditary haemorrhagic telangiectasia -- Rendu-Osler-Weber disease -- ENG -- ALK-1 -- phenotype-genotype relation -- arteriovenous malformation 1