SRY mutation analysis by next generation (deep) sequencing in a cohort of chromosomal Disorders of Sex Development (DSD) patients with a mosaic karyotype
© Hersmus et al.; licensee BioMed Central Ltd. 2012
Received: 8 March 2012
Accepted: 7 November 2012
Published: 16 November 2012
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|8 Mar 2012||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|8 Mar 2012||Author responded||Author comments - Remko Hersmus|
|Resubmission - Version 3|
|8 Mar 2012||Submitted||Manuscript version 3|
|15 May 2012||Reviewed||Reviewer Report - Mark Samuels|
|9 Jul 2012||Reviewed||Reviewer Report - Ken McElreavey|
|19 Jul 2012||Author responded||Author comments - Remko Hersmus|
|Resubmission - Version 4|
|19 Jul 2012||Submitted||Manuscript version 4|
|23 Jul 2012||Reviewed||Reviewer Report - Mark Samuels|
|18 Sep 2012||Author responded||Author comments - Remko Hersmus|
|Resubmission - Version 5|
|18 Sep 2012||Submitted||Manuscript version 5|
|1 Nov 2012||Reviewed||Reviewer Report - Mark Samuels|
|Resubmission - Version 6|
|Submitted||Manuscript version 6|
|7 Nov 2012||Editorially accepted|
|16 Nov 2012||Article published||10.1186/1471-2350-13-108|
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