Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|17 Aug 2017||Submitted||Original manuscript|
|23 Aug 2017||Author responded||Author comments - Zi-Ye ZHAO|
|Resubmission - Version 2|
|23 Aug 2017||Submitted||Manuscript version 2|
|18 Sep 2017||Author responded||Author comments - Zi-Ye ZHAO|
|Resubmission - Version 3|
|18 Sep 2017||Submitted||Manuscript version 3|
|27 Sep 2017||Editorially accepted|
|15 Nov 2017||Article published||10.1186/s12881-017-0471-y|
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