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Xp22.3-p22.1 OMIM PubMed [Amelogenesis imperfecta] Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1 *Gene map locus Xp22.3-p22.1 Amelogenesis imperfecta, X-linked 1 Enamel hypoplasia, X-linked [Clinical features: hypoplastic amelogenesis imperfecta; thin enamel] [Inheritance: X-linked dominant] |