Familial Cancer - 2002
24 articles | Last updated: 2025-12-03 14:12:56
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| Impact of a Cancer Registry-Based Genealogy Service to Support Clinical Genetics Services |
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| A Homozygous MSH6 Mutation in a Child with Café-au-Lait Spots, Oligodendroglioma and Rectal Cancer |
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| Abstracts of the ESO Inside Track Conference on Familial Cancer, CNIO, Madrid, Spain, 6–7 May 2004 |
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| HNPCC and Sporadic MSI-H Colorectal Cancer: A Review of the Morphological Similarities and Differences |
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| Evaluation of Psychosocial Effects of Pre-Symptomatic Testing for Breast/Ovarian and Colon Cancer Pre-Disposing Genes: A 12-Month Follow-Up |
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| Prognosis in DNA Mismatch Repair Deficient Colorectal Cancer: are all MSI Tumours Equivalent? |
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| Genotyping Possible Polymorphic Variants of Human Mismatch Repair Genes in Healthy Korean Individuals and Sporadic Colorectal Cancer Patients |
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| Promoter Hypermethylation Frequency and BRAF Mutations Distinguish Hereditary Non-Polyposis Colon Cancer from Sporadic MSI-H Colon Cancer |
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| Correlations between Phenotype and Microsatellite Instability in HNPCC: Implications for Genetic Testing |
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| Abstracts Presented at the XVIIth Symposium ‘New Developments in Hereditary Cancer’, 5–6 February 2004, Amsterdam, the Netherlands |
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| Sporadic Versus Hereditary forms of Colorectal Cancer with the DNA Microsatellite Instability Phenotype: to ‘lump’ or ‘Split’? |
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| Health economics and genetic service development: a familial cancer genetic example |
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| Patients' and professionals' opinions of services for people at an increased risk of colorectal cancer: an exploratory qualitative study |
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| BRCA1 testing with definitive results: a prospective study of psychological distress in a large clinic-based sample |
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| The 1100delAT BRCA1 and the 8765delAG BRCA2 Mutations: Occurrence in High-Risk Non-Ashkenazi Jews and Haplotype Comparison of Jewish and Non-Jewish Carriers |
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| Delivering Information about Cancer Genetics via Letter to Patients at Low and Moderate Risk of Familial Cancer: A Pilot Study in Wales |
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| Frequency of extra-colonic tumors in hereditary nonpolyposis colorectal cancer (HNPCC) and familial colorectal cancer (FCC) Brazilian families: An analysis by a Brazilian Hereditary Colorectal Cancer |
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| Cancer variation associated with the position of the mutation in the BRCA2 gene |
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| An audit of screening for familial breast cancer before 50 years in the South Thames Region – have we got it right? |
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| BRCA1 testing in breast and/or ovarian cancer families from northeastern France identifies two common mutations with a founder effect |
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| Familial Pancreatic Cancer |
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| Intron 4 Mutation in APC Gene Results in Splice Defect and Attenuated FAP Phenotype |
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| Familial Cancer 2003 – Research and Practice, Couran Cove, Queensland, Australia, 3–6 September 2003 |
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| Instructions for authors |
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