Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS)
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|13 Aug 2018||Submitted||Original manuscript|
|18 Sep 2018||Reviewed||Reviewer Report - Magdalena Ratajska|
|20 Sep 2018||Reviewed||Reviewer Report - Evgeny Imyanitov|
|1 Nov 2018||Author responded||Author comments - Marta Ramírez-Calvo|
|Resubmission - Version 2|
|1 Nov 2018||Submitted||Manuscript version 2|
|18 Nov 2018||Reviewed||Reviewer Report - Magdalena Ratajska|
|8 Jan 2019||Reviewed||Reviewer Report - Evgeny Imyanitov|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|9 Jan 2019||Editorially accepted|
|18 Jan 2019||Article published||10.1186/s13053-019-0104-x|
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