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Peer Review reports

From: Exome sequencing revealed a novel homozygous variant in TRMT61 A in a multiplex family with atypical Cornelia de Lange Syndrome from Rwanda

Original Submission
28 Jan 2025 Submitted Original manuscript
14 Feb 2025 Author responded Author comments - Ambroise Wonkam
Resubmission - Version 2
14 Feb 2025 Submitted Manuscript version 2
23 Mar 2025 Reviewed Reviewer Report
5 Apr 2025 Reviewed Reviewer Report
22 Apr 2025 Author responded Author comments - Ambroise Wonkam
Resubmission - Version 3
22 Apr 2025 Submitted Manuscript version 3
25 Apr 2025 Reviewed Reviewer Report
4 May 2025 Reviewed Reviewer Report
Resubmission - Version 4
Submitted Manuscript version 4
Publishing
6 May 2025 Editorially accepted
13 May 2025 Article published 10.1186/s12920-025-02153-0

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