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

類似資料

• Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening
  著者:: Smith, A, 等
  出版事項: (2007)
• Non-random transmission of mutant alleles to female offspring in BRCA carriers
  著者:: Evans, D, 等
  出版事項: (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
  著者:: Evans, D Gareth, 等
  出版事項: (2008)
• Parity and breast cancer risk among BRCA1 and BRCA2 mutation carriers
  著者:: Antoniou, Antonis C, 等
  出版事項: (2006)
• Women with neurofibromatosis 1 are at a moderately increased risk of developing breast cancer and should be considered for early screening
  著者:: Sharif, S, 等
  出版事項: (2007)