Peer review reports
From: Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly
Original Submission |
15 Jul 2016 |
Submitted |
Original manuscript
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Author responded |
Author comments
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Reviewed |
Reviewer Report
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Resubmission - Version 2 |
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Submitted |
Manuscript version 2
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Author responded |
Author comments
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Resubmission - Version 3 |
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Submitted |
Manuscript version 3
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Publishing |
24 Nov 2016 |
Editorially accepted |
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3 Dec 2016 |
Article published |
10.1186/s12881-016-0355-6
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