Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability.
about
Compound heterozygosity for two MSH2 mutations suggests mild consequences of the initiation codon variant c.1A>G of MSH2.Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers.Tumours with loss of MSH6 expression are MSI-H when screened with a pentaplex of five mononucleotide repeats.Role of microsatellite instability-low as a diagnostic biomarker of Lynch syndrome in colorectal cancer.Patients with an unexplained microsatellite instable tumour have a low risk of familial cancerSimple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndrome.
P2860
Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability.
description
2006 nî lūn-bûn
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2006年の論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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name
Very low prevalence of germlin ...... ut microsatellite instability.
@ast
Very low prevalence of germlin ...... ut microsatellite instability.
@en
type
label
Very low prevalence of germlin ...... ut microsatellite instability.
@ast
Very low prevalence of germlin ...... ut microsatellite instability.
@en
prefLabel
Very low prevalence of germlin ...... ut microsatellite instability.
@ast
Very low prevalence of germlin ...... ut microsatellite instability.
@en
P2093
P2860
P356
P1476
Very low prevalence of germlin ...... ut microsatellite instability.
@en
P2093
Brunner HG
Goossens M
Ligtenberg MJ
Wezenberg SJ
van Krieken JH
P2860
P2888
P304
P356
10.1038/SJ.BJC.6603478
P407
P577
2006-11-21T00:00:00Z