Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report
Pre-publication versions of this article are available by contacting email@example.com.
|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|
|28 Dec 2018||Editorially accepted|
|10 Jan 2019||Article published||10.1186/s12920-018-0471-6|
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