Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literature
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|6 Sep 2011||Submitted||Original manuscript|
|6 Sep 2011||Author responded||Author comments - Anat Erdreich-Epstein|
|Resubmission - Version 2|
|6 Sep 2011||Submitted||Manuscript version 2|
|26 Oct 2011||Reviewed||Reviewer Report - D Gareth Evans|
|19 Dec 2011||Reviewed||Reviewer Report - Concepción Hernández-Chico|
|21 Jan 2012||Author responded||Author comments - Anat Erdreich-Epstein|
|Resubmission - Version 3|
|21 Jan 2012||Submitted||Manuscript version 3|
|27 Jan 2012||Reviewed||Reviewer Report - D Gareth Evans|
|3 Feb 2012||Reviewed||Reviewer Report - Concepción Hernández-Chico|
|Resubmission - Version 4|
|Submitted||Manuscript version 4|
|22 Mar 2012||Editorially accepted|
|22 Mar 2012||Article published||10.1186/1471-2350-13-19|
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