Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report

Peer Review reports

Original Submission
10 Oct 2018	Submitted	Original manuscript
30 Oct 2018	Reviewed	Reviewer Report - Arend B Bökenkamp
2 Nov 2018	Reviewed	Reviewer Report - Felix Claverie-Martin
3 Dec 2018	Author responded	Author comments - Magdalena Danyel
Resubmission - Version 2
3 Dec 2018	Submitted	Manuscript version 2
6 Dec 2018	Reviewed	Reviewer Report - Arend B Bökenkamp
10 Dec 2018	Reviewed	Reviewer Report - Felix Claverie-Martin
26 Dec 2018	Author responded	Author comments - Magdalena Danyel
Resubmission - Version 3
26 Dec 2018	Submitted	Manuscript version 3
Publishing
28 Dec 2018	Editorially accepted
10 Jan 2019	Article published	10.1186/s12920-018-0471-6

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