@article{article, title  = {{Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome}},

 url = {{http://eprints.whiterose.ac.uk/101841/ }},

 year = {{2016}},

 month = {{3}},

 author = {{Hempel A and Pagnamenta AT and Blyth M and Mansour S and McConnell V and Kou I and Ikegawa S and Tsurusaki Y and Matsumoto N and Lo-Castro A and Plessis G et al}},

 doi = {{10.1136/jmedgenet-2015-103393}},

 volume = {{53}},

 journal = {{Journal of Medical Genetics}},

 issue = {{3}},

 pages = {{152-162}},

 note = {{Accessed on 2024/12/22}}}