The genetics of familial breast cancer and their practical implications
- 1 January 1994
- journal article
- review article
- Published by Elsevier in European Journal Of Cancer
- Vol. 30 (9), 1383-1390
- https://doi.org/10.1016/0959-8049(94)90190-2
Abstract
No abstract availableThis publication has 45 references indexed in Scilit:
- Mutation of a mutL Homolog in Hereditary Colon CancerScience, 1994
- The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancerCell, 1993
- Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancerCell, 1993
- Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12–21: exclusion of candidate genes EDH17B2 and RARAHuman Molecular Genetics, 1993
- A second-generation linkage map of the human genomeNature, 1992
- Familial breast-ovarian cancer locus on chromosome 17q12-q23The Lancet, 1991
- Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21Science, 1990
- Risk of cancer death in first-degree relatives of patients with hereditary non-polyposis cancer syndrome (Lynch type II): A study of 130 kindreds in the United KingdomBritish Journal of Surgery, 1990
- AGE AT ONSET AS AN INDICATOR OF FAMILIAL RISK OF BREAST CANCERAmerican Journal of Epidemiology, 1990
- PRACTICAL GUIDE FOR ESTIMATING RISK FOR FAMILIAL BREAST CANCERThe Lancet, 1983