Penetrance of HNPCC-related cancers in a retrolective cohort of 12 large Newfoundland families carrying a MSH2 founder mutation: an evaluation using modified segregation models
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* Corresponding author: Karen A Kopciuk kakopciu@ucalgary.ca
Hereditary Cancer in Clinical Practice 2009, 7:16 doi:10.1186/1897-4287-7-16
Pre-publication versions of this article and reviewers' reports
| Original Submission - Version 1 | Manuscript | 07 Jul 2009 | |
| Reviewer's Report | Catherine Bonaïti-Pellié | 28 Jul 2009 | |
| Reviewer's Report | David Goldgar | 03 Aug 2009 | |
| Resubmission - Version 2 | Manuscript | Author's comment | 15 Sep 2009 |
| Reviewer's Report | David Goldgar | 02 Oct 2009 | |
| Reviewer's Report | Catherine Bonaïti-Pellié | 05 Oct 2009 | |
| Editorial acceptance | 07 Oct 2009 | ||
| Published | 28 Oct 2009 |