Clinical diagnostic exome evaluation for an infant with a lethal disorder: genetic diagnosis of TARP syndrome and expansion of the phenotype in a patient with a newly reported RBM10 alteration

Peer Review reports

Original Submission
24 Jun 2016	Submitted	Original manuscript
11 Oct 2016	Reviewed	Reviewer Report - Bert Callewaert
6 Nov 2016	Reviewed	Reviewer Report - Chiara Bacchelli
21 Dec 2016	Author responded	Author comments - Zoe Powis
Resubmission - Version 2
21 Dec 2016	Submitted	Manuscript version 2
25 Apr 2017	Reviewed	Reviewer Report - Bert Callewaert
18 May 2017	Author responded	Author comments - Zoe Powis
Resubmission - Version 3
18 May 2017	Submitted	Manuscript version 3
Publishing
22 May 2017	Editorially accepted
2 Jun 2017	Article published	10.1186/s12881-017-0426-3

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