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Peer Review reports

From: Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)

Original Submission
24 Aug 2018 Submitted Original manuscript
24 Sep 2018 Reviewed Reviewer Report - Jenny Hewison
28 Sep 2018 Author responded Author comments - Gordon KC Leung
Resubmission - Version 2
28 Sep 2018 Submitted Manuscript version 2
1 Oct 2018 Editorially accepted
25 Oct 2018 Article published 10.1186/s12920-018-0409-z

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