Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families.

Схожие документы

• Haplotype analysis suggest common founders in carriers of the recurrent BRCA2 mutation, 3398delAAAAG, in French Canadian hereditary breast and/ovarian cancer families
  по: Oros, Kathleen K, et al.
  Опубликовано: (2006)
• Double PALB2 and BRCA1/BRCA2 mutation carriers are rare in breast cancer and breast-ovarian cancer syndrome families from the French Canadian founder population
  по: ANCOT, FRÉDÉRIC, et al.
  Опубликовано: (2015)
• Founder BRCA1/BRCA2/PALB2 pathogenic variants in French-Canadian breast cancer cases and controls
  по: Behl, Supriya, et al.
  Опубликовано: (2020)
• Contribution of the PALB2 c.2323C>T [p.Q775X] Founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent
  по: Tischkowitz, Marc, et al.
  Опубликовано: (2013)
• Haplotype analysis of TP53 polymorphisms, Arg72Pro and Ins16, in BRCA1 and BRCA2 mutation carriers of French Canadian descent
  по: Cavallone, Luca, et al.
  Опубликовано: (2008)