Article
Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13.
Oncogene - 20 Apr 1995
Collins N, McManus R, Wooster R, Mangion J, Seal S, Lakhani S R, Ormiston W, Daly P A, Ford D, Easton D F
Abstract excerpt
A small proportion of breast cancer is attributable to the inheritance of dominant, high penetrance susceptibility genes. One of these genes, BRCA2, has recently been localised by genetic linkage analysis to chromosome 13q12-13. This is a region known to exhibit loss of heterozygosity in 20-40% sporadic breast cancers. In this study, we have examined cancers from a family showing strong evidence of linkage to...
Topics
- Alleles
- BRCA2 Protein
- Breast Neoplasms
- Chromosome Deletion
- Chromosomes, Human, Pair 13
- Female
- Genes, Tumor Suppressor
- Genetic Linkage
- Humans
- Neoplasm Proteins
- Transcription Factors
