PH
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| A new bioinformatics tool to help assess the significance of BRCA1 variants | Human Genomics |  | 2018 | 530 | 217 | ||
| Le syndrome de Lynch: pathologiste et praticien peuvent ensemble réduire le risque de cancer | Revue médicale suisse |  | 2011 | 504 | 0 | ||
| Double frameshift mutations in APC and MSH2 in the same individual | International journal of colorectal disease | | 2006 | 841 | 0 | ||
| Double frameshift mutations in APC and MSH2 in the same individual | International journal of colorectal disease | | 2005 | 821 | 0 | ||
| The TPTE gene family: cellular expression, subcellular localization and alternative splicing | Gene | | 2003 | 709 | 0 | ||
| Prostate cancer is part of the hereditary non-polyposis colorectal cancer (HNPCC) tumor spectrum | American journal of medical genetics. Part A | | 2003 | 764 | 0 | ||
| Differential rates of frameshift alterations in four repeat sequences of hereditary nonpolyposis colorectal cancer tumors | Human genetics | | 2002 | 581 | 1 | ||
| The murine orthologue of the Golgi-localized TPTE protein provides clues to the evolutionary history of the human TPTE gene family | Human genetics | | 2001 | 597 | 340 | ||
| Prise en charge multidisciplinaire du cancer colorectal héréditaire | Swiss surgery | | 2001 | 854 | 0 | ||
| Molecular and clinical characteristics in 32 families affected with familial adenomatous polyposis | Human mutation | | 2001 | 762 | 0 | ||
| Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation | Journal of medical genetics | | 1996 | 577 | 0 | ||
| Two novel mutations affecting mRNA splicing of the neurofibromatosis type 1 (NF1) gene | Human mutation | | 1996 | 643 | 0 | ||
| Molecular analysis of a candidate gene for the reproductive isolation between sibling species of Drosophila | Experientia | | 1994 | 123 | 171 |
