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PubMed 10021369 Identification of APC2, a homologue of the adenomatous polyposis coli tumour suppressor. The adenoma 1.07 KB 2019-12-21 13 5 2025-02-21
PubMed 10192393 A common human skin tumour is caused by activating mutations in beta-catenin. WNT signalling orchest 1.72 KB 2015-10-29 12 11 2025-02-21
PubMed 10051005 A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, 2.23 KB 2015-11-01 12 16 2025-02-21
PubMed 10051007 Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal C 1.12 KB 2015-11-01 13 9 2025-02-21
PubMed 100562 Familial deficiency of the seventh component of complement associated with recurrent bacteremic infe 1.43 KB 2015-11-02 16 13 2025-02-21
PubMed 10064668 Increased incidence of cancer in patients with cartilage-hair hypoplasia. OBJECTIVE: Previous report 1.35 KB 2015-11-02 10 17 2025-02-21
PubMed 10071185 Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency. Dihydropyrimidin 1.27 KB 2015-11-02 9 10 2025-02-21
PubMed 10071193 Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the B 1.52 KB 2015-11-02 18 7 2025-02-21
PubMed 10072428 Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cance 1.68 KB 2015-11-02 11 19 2025-02-21
PubMed 10077614 A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Den 1.5 KB 2015-11-04 10 17 2025-02-21