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. Author manuscript; available in PMC: 2015 Oct 23.
Published in final edited form as: Orthod Craniofac Res. 2009 Aug;12(3):212–220. doi: 10.1111/j.1601-6343.2009.01455.x

Fig. 2.

Fig. 2

Amelogenesis imperfecta summary. Genes for which mutations have been identified for each of the Mendelian modes of transmission are illustrated. Clinical photographs illustrating representative examples for each form of Mendelian transmission for AI are shown. The genetic mutation responsible for each case is indicated directly below each photograph. ARAI, autosomal recessive AI; ADAI, autosomal dominant AI; XLAI, X-linked AI).