Quantifying the utility of single nucleotide polymorphisms to guide colorectal cancer screening

Lignende værker

• Perceived versus predicted risks of colorectal cancer and self-reported colonoscopies by members of mismatch repair gene mutation-carrying familieswho have declined genetic testing
  af: Flander, Louisa, et al.
  Udgivet: (2013)
• Response
  af: Ait Ouakrim, Driss, et al.
  Udgivet: (2015)
• P-236 Screening practices of Australians at population and familial risk following the partial roll-out of the National Bowel Cancer Screening Program, 2009-2012
  af: Flander, L., et al.
  Udgivet: (2016)
• Screening practices of unaffected people at familial risk of colorectal cancer Authors
  af: Ait Ouakrim, Driss, et al.
  Udgivet: (2011)
• Screening practices of Australian men and women categorised as “at or slightly above average risk” of colorectal cancer
  af: OUAKRIM, Driss AIT, et al.
  Udgivet: (2012)