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Peer Review reports

From: The most 5′ truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: a case report

Original Submission
25 Jan 2018 Submitted Original manuscript
3 May 2018 Reviewed Reviewer Report - Mahim Jain
9 May 2018 Reviewed Reviewer Report - Jose Caparros-Martin
12 May 2018 Reviewed Reviewer Report - Sheela Nampoothiri
2 Jun 2018 Author responded Author comments - Chulaluck Kuptanon
Resubmission - Version 2
2 Jun 2018 Submitted Manuscript version 2
17 Jun 2018 Reviewed Reviewer Report - Jose Caparros-Martin
19 Jun 2018 Reviewed Reviewer Report - Sheela Nampoothiri
26 Jun 2018 Reviewed Reviewer Report - Mahim Jain
1 Jul 2018 Author responded Author comments - Chulaluck Kuptanon
Resubmission - Version 3
1 Jul 2018 Submitted Manuscript version 3
Publishing
3 Jul 2018 Editorially accepted
16 Jul 2018 Article published 10.1186/s12881-018-0639-0

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