Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes (Q28248540)

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Elisabeth Mangold

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Marlies Sengteller

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Nicolaus Friedrichs

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Stefan Aretz

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Waltraut Friedl

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Constanze Pagenstecher

European Journal of Human Genetics

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language of work or name

English

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publication date

August 2005

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published in

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volume

13

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issue

8

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page(s)

983-6

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cites work

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Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes

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Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.

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Hereditary colorectal cancer

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MSH2 genomic deletions are a frequent cause of HNPCC

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A modified multiplex PCR assay for detection of large deletions in MSH2 and MLH1

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Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer

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