Identification of genetic variants for clinical management of familial colorectal tumors

類似資料

• Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds
  著者:: Dominguez-Valentin, Mev, 等
  出版事項: (2018)
• Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing
  著者:: Dominguez-Valentin, Mev, 等
  出版事項: (2019)
• Automated amplicon design suitable for analysis of DNA variants by melting techniques
  著者:: Ekstrøm, Per Olaf, 等
  出版事項: (2015)
• Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift
  著者:: Møller, Pål, 等
  出版事項: (2019)
• 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
  著者:: Møller, Pål, 等
  出版事項: (2020)