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Peer Review reports

From: Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report

Original Submission
15 Oct 2018 Submitted Original manuscript
14 Nov 2018 Reviewed Reviewer Report - Ilaria Parenti
20 Nov 2018 Reviewed Reviewer Report - Palma Finelli
7 Dec 2018 Author responded Author comments - Rita Alves
Resubmission - Version 2
7 Dec 2018 Submitted Manuscript version 2
26 Dec 2018 Author responded Author comments - Rita Alves
Resubmission - Version 3
26 Dec 2018 Submitted Manuscript version 3
Publishing
3 Jan 2019 Editorially accepted
14 Jan 2019 Article published 10.1186/s12881-019-0745-7

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