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Colon-specific phenotype in Lynch syndrome associated with EPCAM deletion
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Published in: | Clinical genetics 2012-07, Vol.82 (1), p.97-99 |
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cites | cdi_FETCH-LOGICAL-c4656-33c2e38aac988db914fc71cfa5c9dd1ab0a063f8a89e25d8f40674c6410f875f3 |
container_end_page | 99 |
container_issue | 1 |
container_start_page | 97 |
container_title | Clinical genetics |
container_volume | 82 |
creator | Grandval, P Baert-Desurmont, S Bonnet, F Bronner, M Buisine, M-P Colas, C Noguchi, T North, M-O Rey, J-M Tinat, J Toulas, C Olschwang, S |
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doi_str_mv | 10.1111/j.1399-0004.2011.01826.x |
format | article |
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subjects | Adult Aged Aged, 80 and over Antigens, Neoplasm - genetics Biological and medical sciences Cell Adhesion Molecules - genetics Colorectal Neoplasms, Hereditary Nonpolyposis - genetics DNA Mismatch Repair - genetics Epithelial Cell Adhesion Molecule Exons Female Fundamental and applied biological sciences. Psychology Gastroenterology. Liver. Pancreas. Abdomen Genetic Testing Genetics of eukaryotes. Biological and molecular evolution Humans Male Medical genetics Medical sciences Middle Aged Molecular and cellular biology Mutation Rate Risk Factors Sequence Deletion Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
title | Colon-specific phenotype in Lynch syndrome associated with EPCAM deletion |
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