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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