Citation Tools

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

Download to a citation manager

Cite this article as:
Hempel A, Pagnamenta AT, Blyth M, et al
Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome