BRCA1 and BRCA2 mutation carriers in the Breast Cancer Family Registry: an open resource for collaborative research

Podobne knjige/članki

• Contribution of large genomic BRCA1 alterations to early-onset breast cancer selected for family history and tumour morphology: a report from The Breast Cancer Family Registry
  od: Smith, Letitia D, et al.
  Izdano: (2011)
• Breast Cancer Risk for Noncarriers of Family-Specific BRCA1 and BRCA2 Mutations: Findings From the Breast Cancer Family Registry
  od: Kurian, Allison W., et al.
  Izdano: (2011)
• Second primary breast cancer in BRCA1 and BRCA2 mutation carriers: 10-year cumulative incidence in the Breast Cancer Family Registry
  od: Menes, Tehillah S., et al.
  Izdano: (2015)
• The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer
  od: John, Esther M, et al.
  Izdano: (2004)
• Diagnostic chest x-rays and breast cancer risk before age 50 years for BRCA1 and BRCA2 mutation carriers
  od: John, Esther M., et al.
  Izdano: (2013)