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4q21 Google OMIM PubMed [Amelogenesis imperfecta] Amelogenesis imperfecta, type IB *Gene map locus 4q21 AI1B AIH2 Amelogenesis imperfecta, hypoplastic local, autosomal dominant Enamel hypoplasia, hereditary localized [Clinical features: hypoplastic amelogenesis imperfecta; horizontal row of pits, linear depressions, or one large hypoplastic area in the enamel with hypocalcification of the enamel adjacent to and below the hypoplastic area] [Inheritance: autosomal dominant] |