scholarly article | Q13442814 |
P2093 | author name string | Wang Y | |
Sauerbruch T | |||
Propping P | |||
Friedl W | |||
Mathiak M | |||
Kruse R | |||
Lamberti C | |||
Caspari R | |||
Jungck M | |||
Malayeri HR | |||
Ruelfs C | |||
P2860 | cites work | Mutations of two PMS homologues in hereditary nonpolyposis colon cancer | Q24318484 |
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hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds | Q28246692 | ||
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The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
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Microsatellite instability in cancer of the proximal colon | Q29620692 | ||
Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria | Q34386209 | ||
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Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations | Q42037545 | ||
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Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene? | Q55670482 | ||
Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients | Q57570041 | ||
Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer | Q61946741 | ||
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Clinical implications of microsatellite instability in colorectal cancers | Q71067454 | ||
Diagnostic use of microsatellite instability in hereditary non-polyposis colorectal cancer | Q71520203 | ||
Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability | Q72127255 | ||
Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients | Q72313890 | ||
A novel approach to estimate the proportion of hereditary nonpolyposis colorectal cancer of total colorectal cancer burden | Q72374029 | ||
Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue | Q73628202 | ||
Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes | Q73701709 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | colorectal cancer | Q188874 |
colorectal carcinoma | Q25493920 | ||
microsatellite | Q265193 | ||
P304 | page(s) | 839-843 | |
P577 | publication date | 1999-06-01 | |
P1433 | published in | Gut | Q5621669 |
P1476 | title | Microsatellite instability-a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer | |
P478 | volume | 44 |