Germline mutations in BRCA1 and BRCA2 account for majority of hereditary breast and ovarian cancer. The complete coding sequence analysis of both genes was carried out in 197 breast/ovarian cancer patients from high-risk families and 53 patients with sporadic breast/ovarian cancer. In summary, 59 mu
β¦ LIBER β¦
BRCA1disease-associated haplotypes in Singapore Malay women with early-onset breast/ovarian cancer
β Scribed by A. B. Ali; P. T. Iau; T. C. Putti; J. H. Sng
- Publisher
- Springer US
- Year
- 2007
- Tongue
- English
- Weight
- 125 KB
- Volume
- 104
- Category
- Article
- ISSN
- 0167-6806
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