This article has Open Peer Review reports available.
Clinical and molecular genetic characterization of familial MECP2 duplication syndrome in a Chinese family
- Xiaoyan Li†1, 2,
- Hua Xie†2, 3,
- Qian Chen4,
- Xiongying Yu1,
- Zhaoshi Yi1,
- Erzhen Li4,
- Ting Zhang2,
- Jian Wang5,
- Jianmin Zhong1Email author and
- Xiaoli Chen2, 3Email authorView ORCID ID profile
© The Author(s). 2017
Received: 17 July 2016
Accepted: 24 October 2017
Published: 15 November 2017
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|17 Jul 2016||Submitted||Original manuscript|
|27 Sep 2016||Reviewed||Reviewer Report - Zilong Qiu|
|17 Oct 2016||Reviewed||Reviewer Report - Helen Leonard|
|25 Nov 2016||Author responded||Author comments - Xiaoyan Li|
|Resubmission - Version 2|
|25 Nov 2016||Submitted||Manuscript version 2|
|6 Feb 2017||Reviewed||Reviewer Report - Helen Leonard|
|6 Mar 2017||Author responded||Author comments - Xiaoyan Li|
|Resubmission - Version 3|
|6 Mar 2017||Submitted||Manuscript version 3|
|20 Oct 2017||Author responded||Author comments - Xiaoyan Li|
|Resubmission - Version 4|
|20 Oct 2017||Submitted||Manuscript version 4|
|24 Oct 2017||Editorially accepted|
|15 Nov 2017||Article published||10.1186/s12881-017-0486-4|
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