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Pre-publication history

Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report

Guillaume de la Houssaye email, Ivan Bieche email, Olivier Roche email, Véronique Vieira email, Ingrid Laurendeau email, Laurence Arbogast email, Hatem Zeghidi email, Philippe Rapp email, Philippe Halimi email, Michel Vidaud email, Jean-Louis Dufier email, Maurice Menasche email and Marc Abitbol email

BMC Medical Genetics 2006, 7:82doi:10.1186/1471-2350-7-82

Pre-publication versions of this article and reviewers' reports

Original submission - Version 1Manuscript10 Aug 2006
Reviewer's ReportTord Hjalt21 Aug 2006
Resubmission - Version 2ManuscriptAuthors' comments30 Aug 2006
Resubmission - Version 3ManuscriptAuthors' comments30 Aug 2006
Resubmission - Version 4ManuscriptAuthors' comments30 Aug 2006
Resubmission - Version 5ManuscriptAuthors' comments30 Aug 2006
Reviewer's ReportDarryl Nishimura12 Sep 2006
Reviewer's ReportTord Hjalt13 Sep 2006
CommentEditor's comment14 Sep 2006
Resubmission - Version 6ManuscriptAuthors' comments30 Sep 2006
Resubmission - Version 7ManuscriptAuthors' comments30 Sep 2006
Reviewer's ReportDarryl Nishimura09 Oct 2006
Reviewer's ReportTord Hjalt10 Oct 2006
Resubmission - Version 8ManuscriptAuthors' comments02 Nov 2006
Resubmission - Version 9ManuscriptAuthors' comments02 Nov 2006
Resubmission - Version 10ManuscriptAuthors' comments02 Nov 2006
Resubmission - Version 11ManuscriptAuthors' comments27 Nov 2006
Resubmission - Version 12ManuscriptAuthors' comments28 Nov 2006
Accepted29 Nov 2006
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