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

Παρόμοια τεκμήρια

• Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift
  ανά: Møller, Pål, κ.ά.
  Έκδοση: (2019)
• Ten modifiers of BRCA1 penetrance validated in a Norwegian series
  ανά: Heramb, Cecilie, κ.ά.
  Έκδοση: (2015)
• The BRCA2 variant c.68-7 T>A is associated with breast cancer
  ανά: Møller, Pål, κ.ά.
  Έκδοση: (2017)
• Retraction Note to: The BRCA2 variant c.68–7 T > A is associated with breast cancer
  ανά: Møller, Pål, κ.ά.
  Έκδοση: (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
  ανά: Borg, Åke, κ.ά.
  Έκδοση: (1999)