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Amelogenesis Imperfecta

Known as: Amelogenesis Imperfecta [Disease/Finding], Congenital Enamel Hypoplasia 
A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL… 
National Institutes of Health

Papers overview

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1997
1997
Mutations in the amelogenin gene, AMGX, are known to cause X-linked amelogenesis imperfecta (AIH1). We have used DNA single… 
1993
1993
Two siblings, the only children of a family, are reported with epilepsy, mental deterioration and yellow teeth because of… 
1993
1993
This study was performed to examine whether a clinical classification of different phenotypes of amelogenesis imperfecta could be… 
Highly Cited
1990
Highly Cited
1990
X-linked Amelogenesis imperfecta (AI) is a genetic disorder affecting the formation of enamel. In the present study two families… 
1973
1973
A Negro girl came to the Emory University Dental School and requested full-mouth extractions. She was found to have amelogenesis… 
Review
1972
Review
1972
The X-linked hypomaturation type of amelogenesis imperfecta was first described by Witkop [1-3] in two kindreds during a survey… 
1972
1972
1971
1971