Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA. (Q52859644)
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scientific article published in December 2003
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English | Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA. |
scientific article published in December 2003 |
Statements
Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA. (English)
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C F Taylor
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R S Charlton
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E Sheridan
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G R Taylor
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1 December 2003
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22
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6
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428-433
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