Catherine Badens

Mutations in PHD‐like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndrome

A. Munnich, N. Philip, H. Van Esch, 2006, Clinical genetics.

In utero seizures revealing dentato‐olivary dysplasia caused by SCN2A mutation

A. Laquérriere, L. Villard, S. Moutton, 2017, Neuropathology and applied neurobiology.

[Next-generation DNA sequencing in clinical diagnostics].

M. Krahn, C. Lacoste, P. Bourgeois, 2017, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.