Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome

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Description scientific article published on 5 November 2015
Author/s

author: Jenny Taylor  Moira Blyth  Usha Kini  Yoshinori Tsurusaki  Alistair T Pagnamenta 

Publication date November 5, 2015
Language English
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