MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development.

Characterizes the chromosome homologue of the Opitz syndrome gene MID1 in terms of subcellular localization and expression during development. Nuclear factors involved in the dorsal-ventral patterning of the embryo; Mode of inheritance; Physical characteristics of persons with epilepsy and mental retardation; Formation of multiprotein complexes.