Co-occurrence of mutations in KIF7 and KIAA0556 in Joubert syndrome with ocular coloboma, pituitary malformation and growth hormone deficiency: a case report and literature review

Peer Review reports

Original Submission
3 Dec 2019	Submitted	Original manuscript
8 Jan 2020	Reviewed	Reviewer Report - Yucai Chen
24 Jan 2020	Reviewed	Reviewer Report - Michele Callea
17 Feb 2020	Author responded	Author comments - Niceta Marcello
20 Feb 2020	Reviewed	Reviewer Report - Yucai Chen
28 Feb 2020	Reviewed	Reviewer Report - Michele Callea
Resubmission - Version 2
17 Feb 2020	Submitted	Manuscript version 2
Publishing
2 Mar 2020	Editorially accepted
12 Mar 2020	Article published	10.1186/s12887-020-2019-0

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