articleThe LancetMar 1, 2004Closed access

A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 ( SMAD4)

CJCarol J. GallioneGMGabriela M. RepettoELEric LegiusAKAnil K. RustgiSSSusan Schelley

Duke University Hospital · Duke Medical Center · +10 more institutions

PubMed
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Abstract

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752
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Authors

10

Topics & keywords

Topics
Keywords
  • Proband
  • ACVRL1
  • Genetics
  • Phenotype
  • Mutation
  • Telangiectasia
  • Biology
  • Telangiectases
UN Sustainable Development Goals
  • Good health and well-being
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