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Peer Review reports

From: Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction

Original Submission
19 Jan 2018 Submitted Original manuscript
19 Feb 2018 Reviewed Reviewer Report - Carl Ernst
27 Feb 2018 Reviewed Reviewer Report - Yin Yao
30 Mar 2018 Author responded Author comments - Elysa Marco
Resubmission - Version 2
30 Mar 2018 Submitted Manuscript version 2
20 Apr 2018 Author responded Author comments - Elysa Marco
Resubmission - Version 3
20 Apr 2018 Submitted Manuscript version 3
Publishing
26 Apr 2018 Editorially accepted
25 May 2018 Article published 10.1186/s12920-018-0362-x

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BMC Medical Genomics

ISSN: 1755-8794

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