A targeted analysis identifies a high frequency of BRCA1 and BRCA2 mutation carriers in women with ovarian cancer from a founder population

Benzer Materyaller

• Double PALB2 and BRCA1/BRCA2 mutation carriers are rare in breast cancer and breast-ovarian cancer syndrome families from the French Canadian founder population
  Yazar:: ANCOT, FRÉDÉRIC, ve diğerleri
  Baskı/Yayın Bilgisi: (2015)
• Haplotype analysis suggest common founders in carriers of the recurrent BRCA2 mutation, 3398delAAAAG, in French Canadian hereditary breast and/ovarian cancer families
  Yazar:: Oros, Kathleen K, ve diğerleri
  Baskı/Yayın Bilgisi: (2006)
• Haplotype analysis of TP53 polymorphisms, Arg72Pro and Ins16, in BRCA1 and BRCA2 mutation carriers of French Canadian descent
  Yazar:: Cavallone, Luca, ve diğerleri
  Baskı/Yayın Bilgisi: (2008)
• Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families.
  Yazar:: Tonin, P N, ve diğerleri
  Baskı/Yayın Bilgisi: (1998)
• Case Review: Whole-Exome Sequencing Analyses Identify Carriers of a Known Likely Pathogenic Intronic <i>BRCA1</i> Variant in Ovarian Cancer Cases Clinically Negative for Pathogenic <i>BRCA1</i> and <i>BRCA2</i> Variants
  Yazar:: Wejdan M. Alenezi, ve diğerleri
  Baskı/Yayın Bilgisi: (2022-04-01)