Figure 4From: Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly MRI of LIS_TUB_011 foetus 23 with lissencephaly with cerebellar hypoplasia at 32 WG with TUBA1A mutation (p.V409A) showing complete agyria, virtually no sulci on axial (a) and coronal (b,d) T2-weighted sections, complete corpus callosum agenesis and pontocerebellar hypoplasia on sagittal (c) and coronal (d) sections. Back to article page