Double PALB2 and BRCA1/BRCA2 mutation carriers are rare in breast cancer and breast-ovarian cancer syndrome families from the French Canadian founder population

Ítems similars

• Founder BRCA1/BRCA2/PALB2 pathogenic variants in French-Canadian breast cancer cases and controls
  per: Behl, Supriya, et al.
  Publicat: (2020)
• Haplotype analysis suggest common founders in carriers of the recurrent BRCA2 mutation, 3398delAAAAG, in French Canadian hereditary breast and/ovarian cancer families
  per: Oros, Kathleen K, et al.
  Publicat: (2006)
• Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families.
  per: Tonin, P N, et al.
  Publicat: (1998)
• Haplotype analysis of TP53 polymorphisms, Arg72Pro and Ins16, in BRCA1 and BRCA2 mutation carriers of French Canadian descent
  per: Cavallone, Luca, et al.
  Publicat: (2008)
• A targeted analysis identifies a high frequency of BRCA1 and BRCA2 mutation carriers in women with ovarian cancer from a founder population
  per: Belanger, Moria H, et al.
  Publicat: (2015)