
Give the Gift of Choice!
Too many options? Treat your friends and family to their favourite stores with a Bayshore Shopping Centre gift card, redeemable at participating retailers throughout the centre. Click below to purchase yours today!Purchase HereHome
Hereditary Breast and Ovarian Cancer Syndrome
Coles
Loading Inventory...
Hereditary Breast and Ovarian Cancer Syndrome in Ottawa, ON
By None
Current price: $63.95


By None
Hereditary Breast and Ovarian Cancer Syndrome in Ottawa, ON
Current price: $63.95
Loading Inventory...
Size: Paperback
*Product information may vary - to confirm product availability, pricing, shipping and return information please contact Coles
Given the high percentage of breast cancer cases with high familial aggregation that are not explained by alterations in the main susceptibility genes, BRCA1 and BRCA2, we proposed this study with the aim of determining the mutational prevalence of the RAD51C gene and the RAD51D gene in our population. These results will be useful for the assessment of RAD51C and RAD51D as risk predictors of hereditary breast and ovarian cancer syndrome (HBCS). For this purpose, a cross-sectional study was performed on patients meeting criteria for high or moderate risk of SCMOH syndrome in whom no pathogenic gene variant in BRCA1, BRCA2 and CHEK2 was found to be associated with increased risk.
Given the high percentage of breast cancer cases with high familial aggregation that are not explained by alterations in the main susceptibility genes, BRCA1 and BRCA2, we proposed this study with the aim of determining the mutational prevalence of the RAD51C gene and the RAD51D gene in our population. These results will be useful for the assessment of RAD51C and RAD51D as risk predictors of hereditary breast and ovarian cancer syndrome (HBCS). For this purpose, a cross-sectional study was performed on patients meeting criteria for high or moderate risk of SCMOH syndrome in whom no pathogenic gene variant in BRCA1, BRCA2 and CHEK2 was found to be associated with increased risk.

















