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Peer Review reports

From: Identification of a novel compound heterozygous SMG9 variants in a Chinese family with heart and brain malformation syndrome using whole exome sequencing

Original Submission
18 Jan 2022 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
12 Feb 2022 Reviewed Reviewer Report - Jianjun Xiong
18 Feb 2022 Reviewed Reviewer Report
20 Feb 2022 Reviewed Reviewer Report
22 Feb 2022 Reviewed Reviewer Report
5 Mar 2022 Author responded Author comments - Jingsi Luo
Resubmission - Version 3
5 Mar 2022 Submitted Manuscript version 3
10 Mar 2022 Reviewed Reviewer Report - Jianjun Xiong
12 Mar 2022 Reviewed Reviewer Report
15 Mar 2022 Author responded Author comments - Jingsi Luo
Resubmission - Version 4
15 Mar 2022 Submitted Manuscript version 4
Publishing
17 Mar 2022 Editorially accepted
23 Mar 2022 Article published 10.1186/s12920-022-01217-9

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