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Peer Review reports

From: Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss

Original Submission
27 Nov 2020 Submitted Original manuscript
21 Dec 2020 Author responded Author comments - Yang Guangxian
Resubmission - Version 2
21 Dec 2020 Submitted Manuscript version 2
26 Aug 2020 Reviewed Reviewer Report
24 Dec 2020 Author responded Author comments - Yang Guangxian
Resubmission - Version 3
24 Dec 2020 Submitted Manuscript version 3
31 Dec 2020 Author responded Author comments - Yang Guangxian
Resubmission - Version 4
31 Dec 2020 Submitted Manuscript version 4
19 Nov 2020 Reviewed Reviewer Report
5 Jan 2021 Author responded Author comments - Yang Guangxian
Resubmission - Version 5
5 Jan 2021 Submitted Manuscript version 5
6 Jan 2021 Author responded Author comments - Yang Guangxian
Resubmission - Version 6
6 Jan 2021 Submitted Manuscript version 6
Publishing
7 Jan 2021 Editorially accepted
21 Jan 2021 Article published 10.1186/s12920-021-00871-9

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