Copy Number Variation Analysis in Familial BRCA1/2-Negative Finnish Breast and Ovarian Cancer

Lignende værker

• Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals
  af: Kuusisto, Kirsi M, et al.
  Udgivet: (2011)
• Whole-exome sequencing of Finnish hereditary breast cancer families
  af: Määttä, Kirsi, et al.
  Udgivet: (2017)
• Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families
  af: Määttä, Kirsi M., et al.
  Udgivet: (2017)
• DNA copy number profiling reveals extensive genomic loss in hereditary BRCA1 and BRCA2 ovarian carcinomas
  af: Kamieniak, M M, et al.
  Udgivet: (2013)
• Genetic, clinic and histopathologic characterization of BRCA-associated hereditary breast and ovarian cancer in southwestern Finland
  af: Terhi Aino-Sofia Pallonen, et al.
  Udgivet: (2022-04-01)