A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features

1. Quintela, I.
2. Barros, F.
3. Lago-Leston, R.
4. Castro-Gago, M.
5. Carracedo, A.
6. Eiris, J.