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Peer Review reports

From: Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations

Original Submission
31 May 2021 Submitted Original manuscript
23 Jun 2021 Author responded Author comments - Somprakash Dhangar
Resubmission - Version 2
23 Jun 2021 Submitted Manuscript version 2
30 Aug 2021 Reviewed Reviewer Report
31 Aug 2021 Reviewed Reviewer Report
28 Sep 2021 Author responded Author comments - Somprakash Dhangar
Resubmission - Version 3
28 Sep 2021 Submitted Manuscript version 3
18 Oct 2021 Author responded Author comments - Somprakash Dhangar
Resubmission - Version 4
18 Oct 2021 Submitted Manuscript version 4
25 Oct 2021 Author responded Author comments - Somprakash Dhangar
Resubmission - Version 5
25 Oct 2021 Submitted Manuscript version 5
29 Oct 2021 Author responded Author comments - Somprakash Dhangar
Resubmission - Version 6
29 Oct 2021 Submitted Manuscript version 6
3 Nov 2021 Author responded Author comments - Somprakash Dhangar
Resubmission - Version 7
3 Nov 2021 Submitted Manuscript version 7
2 Dec 2021 Author responded Author comments - Somprakash Dhangar
Resubmission - Version 8
2 Dec 2021 Submitted Manuscript version 8
9 Dec 2021 Author responded Author comments - Somprakash Dhangar
Resubmission - Version 9
9 Dec 2021 Submitted Manuscript version 9
14 Dec 2021 Author responded Author comments - Somprakash Dhangar
Resubmission - Version 10
14 Dec 2021 Submitted Manuscript version 10
Publishing
20 Dec 2021 Editorially accepted
3 Jan 2022 Article published 10.1186/s12920-021-01152-1

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