Response to correspondence on “Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening”

Схожие документы

• Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening
  по: Smith, A, et al.
  Опубликовано: (2007)
• Non-random transmission of mutant alleles to female offspring in BRCA carriers
  по: Evans, D, et al.
  Опубликовано: (2005)
• Penetrance estimates for BRCA1 and BRCA2 based on genetic testing in a Clinical Cancer Genetics service setting: Risks of breast/ovarian cancer quoted should reflect the cancer burden in the family
  по: Evans, D Gareth, et al.
  Опубликовано: (2008)
• Parity and breast cancer risk among BRCA1 and BRCA2 mutation carriers
  по: Antoniou, Antonis C, et al.
  Опубликовано: (2006)
• Phenocopies in breast cancer 1 (BRCA1) families: implications for genetic counselling
  по: Gronwald, Jacek, et al.
  Опубликовано: (2007)