AIH3Amelogenesis Imperfecta 3, Hypoplastic Type
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For example a second locus for X-linked recessive AI, (AIH3) has been mapped to chromosome Xq24-q27.1 Similarly, an autosomal dominant, local hypoplastic form of AI, (AIH2) has been mapped to a 4mb region of human chromosome 4q11-q21 that encompasses the gene encoding the amleoblast specific protein ameloblastin, AMBN.
Clinical features of a family with X-linked amelogenesis imperfecta mapping to a new locus (AIH3) on the long arm of the x chromosome.