{"id":"W2131246162","doi":"10.1016/s0140-6736(04)15732-2","title":"A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 ( SMAD4)","year":2004,"lang":"en","type":"article","venue":"The Lancet","topic":"Vascular Anomalies and Treatments","field":"Medicine","cited_by":754,"is_retracted":false,"has_abstract":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine","funders":"National Heart, Lung, and Blood Institute; National Institutes of Health; Vlaamse regering; Fonds Wetenschappelijk Onderzoek","keywords":"Proband; ACVRL1; Genetics; Phenotype; Mutation; Telangiectasia; Biology; Telangiectases; Endoglin; Medicine; Pathology; Gene","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":null,"machine_scores":{"provisional":true,"baseline":true,"maturity_gate_passed":false,"score_opus":0.01656213724542048,"score_gpt":0.2417285971790504,"score_spread":0.2251664599336299,"validation_status":"score_only:v0-immature-baseline","note":"Baseline scores from an immature model (maturity gate not passed). Scores rank; they never assert a category."}}