Hereditary Cancer in Clinical Practice


Open Access Pre-publication history

A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome

Els van Riel*, Margreet GEM Ausems, Frans BL Hogervorst, Irma Kluijt, Marielle E van Gijn, Jeanne van Echtelt, Karen Scheidel-Jacobse, Eric FAM Hennekam, Rein P Stulp, Yvonne J Vos, G Johan A Offerhaus, Fred H Menko and Johan JP Gille

Hereditary Cancer in Clinical Practice 2010, 8:7 doi:10.1186/1897-4287-8-7

Pre-publication versions of this article and reviewers' reports

Original Submission - Version 1 Manuscript 07 May 2010
Reviewer's Report Paivi Peltomaki 04 Jun 2010
Reviewer's Report hans morreau 15 Jun 2010
Resubmission - Version 2 Manuscript Author's comment 16 Jul 2010
Editorial acceptance 26 Jul 2010
Published 12 Aug 2010