TY  - JOUR

T1  - Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome

JO  - Journal of Medical Genetics

UR  - https://eprints.whiterose.ac.uk/id/eprint/101841

UR  - http://dx.doi.org/10.1136/jmedgenet-2015-103393

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

PB  - BMJ Publishing Group

VL  - 53

IS  - 3

SP  - 152

EP  - 162

Y2  - 2025/11/03

ER  -