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
Language | Label | Description | Also known as |
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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)
C F Taylor
R S Charlton
E Sheridan
G R Taylor
1 December 2003
22
6
428-433