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source DB |
source ID
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text
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size
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updated at |
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# proj.
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# Ann.
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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 |
2025-01-16
|
| 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 |
|
14 |
2025-01-16
|
| PubMed |
10051005 |
A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, |
2.23 KB |
2015-11-01 |
|
12 |
|
17 |
2025-01-16
|
| 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 |
|
11 |
2025-01-16
|
| PubMed |
100562 |
Familial deficiency of the seventh component of complement associated with recurrent bacteremic infe |
1.43 KB |
2015-11-02 |
|
16 |
|
12 |
2025-01-16
|
| PubMed |
10064668 |
Increased incidence of cancer in patients with cartilage-hair hypoplasia.
OBJECTIVE: Previous report |
1.35 KB |
2015-11-02 |
|
10 |
|
17 |
2025-01-16
|
| PubMed |
10071185 |
Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency.
Dihydropyrimidin |
1.27 KB |
2015-11-02 |
|
9 |
|
11 |
2025-01-16
|
| PubMed |
10071193 |
Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the B |
1.52 KB |
2015-11-02 |
|
18 |
|
8 |
2025-01-16
|
| PubMed |
10072428 |
Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cance |
1.68 KB |
2015-11-02 |
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11 |
|
16 |
2025-01-16
|
| PubMed |
10077614 |
A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Den |
1.5 KB |
2015-11-04 |
|
10 |
|
27 |
2025-01-16
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