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Peer Review reports

From: Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations

Original Submission
18 Sep 2019 Submitted Original manuscript
23 Oct 2019 Author responded Author comments - Jeevana Praharsha
29 Nov 2019 Reviewed Reviewer Report - Bradley Miller
9 Dec 2019 Reviewed Reviewer Report - Alexsandra C. Malaquias
11 Dec 2019 Reviewed Reviewer Report - Luis Pablo Gravina
10 Jan 2020 Author responded Author comments - Jeevana Praharsha
Resubmission - Version 2
23 Oct 2019 Submitted Manuscript version 2
21 Jan 2020 Author responded Author comments - Jeevana Praharsha
Resubmission - Version 3
21 Jan 2020 Submitted Manuscript version 3
6 Feb 2020 Author responded Author comments - Jeevana Praharsha
Resubmission - Version 4
6 Feb 2020 Submitted Manuscript version 4
11 Feb 2020 Author responded Author comments - Jeevana Praharsha
Resubmission - Version 5
11 Feb 2020 Submitted Manuscript version 5
13 Feb 2020 Author responded Author comments - Jeevana Praharsha
Resubmission - Version 6
13 Feb 2020 Submitted Manuscript version 6
17 Feb 2020 Author responded Author comments - Jeevana Praharsha
Resubmission - Version 7
17 Feb 2020 Submitted Manuscript version 7
20 Feb 2020 Author responded Author comments - Jeevana Praharsha
Resubmission - Version 8
20 Feb 2020 Submitted Manuscript version 8
Publishing
25 Feb 2020 Editorially accepted
12 Mar 2020 Article published 10.1186/s12881-020-0986-5

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