Open Access Highly Accessed Pre-publication history

SRY mutation analysis by next generation (deep) sequencing in a cohort of chromosomal Disorders of Sex Development (DSD) patients with a mosaic karyotype

Remko Hersmus, Hans Stoop, Erin Turbitt, J Wolter Oosterhuis, Stenvert LS Drop, Andrew H Sinclair, Stefan J White and Leendert HJ Looijenga*

BMC Medical Genetics 2012, 13:108  doi:10.1186/1471-2350-13-108

Pre-publication versions of this article and reviewers' reports

Original Submission - Version 1 Manuscript 08 Mar 2012
Resubmission - Version 2 Manuscript Author's comment 08 Mar 2012
Reviewer's Report Mark Samuels 15 May 2012
Reviewer's Report Ken McElreavey 09 Jul 2012
Resubmission - Version 3 Manuscript Author's comment 19 Jul 2012
Reviewer's Report Mark Samuels 23 Jul 2012
Resubmission - Version 4 Manuscript Author's comment 18 Sep 2012
Reviewer's Report Mark Samuels 01 Nov 2012
Editorial acceptance 07 Nov 2012
Published 16 Nov 2012