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The molecular cascades that control craniofacial development have until recently been little understood. The paucity of data that exists has in part been due to the complexity of the head, which is a unique, and possibly one of the most intricate regions of the body. However, the generation of mouse mutants, the identification of gene mutations that cause human craniofacial syndromes, together with classical embryological approaches in other species has now given significant insight how the head develops.
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