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NCBI-Disease-Corpus-4oGuideline-All
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# Ann.
updated_at
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
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