TY - JOUR T1 - Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin鈥揝iris syndrome JO - Journal of Medical Genetics UR - http://eprints.whiterose.ac.uk/101841/ PY - 2016/03/01 AU - Hempel A AU - Pagnamenta AT AU - Blyth M AU - Mansour S AU - McConnell V AU - Kou I AU - Ikegawa S AU - Tsurusaki Y AU - Matsumoto N AU - Lo-Castro A AU - Plessis G et al ED - DO - DOI: 10.1136/jmedgenet-2015-103393 VL - 53 IS - 3 SP - 152 EP - 162 Y2 - 2025/07/06 ER -