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]

Hypomaturation Amelogenesis Imperfecta: Account of a Family with an X-linked Inheritance Pattern
Hypomaturation Amelogenesis Imperfecta: Account of a Family with an X-linked Inheritance Pattern
Hypomaturation Amelogenesis Imperfecta: Account of a Family with an X-linked Inheritance Pattern
Brazilian Dental Journal
Brazilian Dental Journal
Brazilian Dental Journal

A Novel Missense Mutation (p.P52R) in Amelogenin Gene Causing X-linked Amelogenesis Imperfecta
Amelogenin p.M1T and p.W4S Mutations Underlying Hypoplastic X-linked Amelogenesis Imperfecta
Amelogenin p.M1T and p.W4S Mutations Underlying Hypoplastic X-linked Amelogenesis Imperfecta
Journal of Dental Research
Journal of Dental Research
Journal of Dental Research


 

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Edited by Aldo Campana, February 8, 2010