The aim of this paper is to evaluate correlative magnetic resonance imaging (MRI) and histological parameters of development of cortical afferents during pathfinding and target selection in transient fetal cerebral laminas in human fetuses and preterm infants. The transient fetal subplate zone, situated between the fetal white matter (i.e. intermediate zone) and the cortical plate, is the crucial laminar compartment for development of thalamocortical and corticocortical afferents. The prolonged coexistence of transient (endogenously active) and permanent (sensorydriven) circuitry within the transient fetal zones is a salient feature of the fetal and preterm cortex; this transient circuitry is the substrate of cerebral functions in preterm infants. Another transient aspect of organization of developing fibre pathways is the abundance of extracellular matrix and guidance molecules in periventricular crossroads of projection and corticocortical pathways. Both the subplate zone and periventricular crossroads are visible on MRI in vivo and in vitro. Hypoxic-ischaemic lesions of periventricular crossroads are the substrate for motor, sensory, and cognitive deficits after focal periventricular leukomalacia (PVL). Lesions of distal portions of the white matter and the subplate zone are the substrate for diffuse PVL. The neuronal elements in transient fetal zones form a developmental potential for plasticity after perinatal cerebral lesions.Our understanding and interpretation of structural and functional consequences of cerebral lesions in human fetuses and preterm infants largely depends on knowledge of neurogenetic cellular events that can be demonstrated by in vivo neuroimaging. A necessary step in this approach is the correlation between magnetic resonance imaging (MRI) and histological organization during different phases of histogenesis. Namely, in the fetal cerebrum, early neurogenetic cellular events (i.e. proliferation, migration, aggregation, cell death, growth of axons, and the establishment of neuronal connections) proceed according to the specific timetable within transient, histologically recognizable fetal zones which do not have an equivalent in the adult brain. 1 During the last third of gestation, neuronal proliferation and migration are mostly completed 1 whereas the development of axonal pathways 2,3 and the differentiation of cortical neurons 4 become the most prominent neurogenetic events. Synaptogenesis continues as the dominant neurogenetic event during postnatal life. In addition to precise timing, these neurogenetic events also display a characteristic spatial occurrence: neuronal proliferation occurs in the ventricular and subventricular zones, whereas neuronal migration and growth of axons occur predominantly in the intermediate zone (the fetal white matter) and the subplate zone, which is situated between the intermediate zone and the cortical plate. 1 Neuronal differentiation and synaptogenesis begin in the transient subplate zone 5 and continue in the cortical plate. 1,5 Recent research in...