Catherine Garel

RELN and VLDLR mutations underlie two distinguishable clinico‐radiological phenotypes

C. Garel, A. Toutain, D. Rodriguez, 2016, Clinical genetics.

Loss-of-function variants in ZEB1 cause dominant anomalies of the corpus callosum with favourable cognitive prognosis

C. Depienne, E. Sherr, E. Blondiaux, 2023, Journal of medical genetics.