John Libbey Eurotext

Epileptic Disorders

The Educational Journal of the International League Against Epilepsy

Benign infantile seizures followed by autistic regression in a boy with 16p11.2 deletion Volume 19, numéro 2, June 2017

Figure 1

Array CGH profile showing the 16p11.2 deletion (arrow) (UCSC genome Browser; http://genome.ucsc.edu/; hg 19 release), with enlargement of the deleted region in the child (A) and his mother (B).