Most familial breast or ovarian cancers are thought to be due to highly penetrant mutations in the predisposing genes BRCA1 and BRCA2. The cloning of these genes has opened a new era for the genetic counseling of women with a family history of breast or ovarian cancer. To estimate the incidence of d
Incidence of BRCA1 and BRCA2 mutations in 54 Chilean families with breast/ovarian cancer, genotype–phenotype correlations
✍ Scribed by Marcela Gallardo; Antonia Silva; Lorena Rubio; Carolina Alvarez; Carolina Torrealba; Mauricio Salinas; Teresa Tapia; Paola Faundez; Lorena Palma; María Eugenia Riccio; Hernando Paredes; Mario Rodriguez; Adolfo Cruz; Christine Rousseau; Mary Claire King; Mauricio Camus; Manuel Alvarez; Pilar Carvallo
- Publisher
- Springer US
- Year
- 2005
- Tongue
- English
- Weight
- 180 KB
- Volume
- 95
- Category
- Article
- ISSN
- 0167-6806
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