Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift

समान संसाधन

• Correction: Møller, P.; et al. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11, 132
  द्वारा: Møller, Pål, और अन्य
  प्रकाशित: (2020)
• Ten modifiers of BRCA1 penetrance validated in a Norwegian series
  द्वारा: Heramb, Cecilie, और अन्य
  प्रकाशित: (2015)
• The BRCA2 variant c.68-7 T>A is associated with breast cancer
  द्वारा: Møller, Pål, और अन्य
  प्रकाशित: (2017)
• Retraction Note to: The BRCA2 variant c.68–7 T > A is associated with breast cancer
  द्वारा: Møller, Pål, और अन्य
  प्रकाशित: (2018)
• BRCA1 1675delA and 1135insA Account for One Third of Norwegian Familial Breast-Ovarian Cancer and Are Associated with Later Disease Onset than Less Frequent Mutations
  द्वारा: Borg, Åke, और अन्य
  प्रकाशित: (1999)