Amelogenesis Imperfecta, Type Ic

Known as: AI1C, Amelogenesis Imperfecta, Hypoplastic, With Or Without Openbite Malocclusion, Autosomal Recessive, Amelogenesis Imperfecta, Local Hypoplastic Type, Autosomal Recessive 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1973-2018
024619732018

Papers overview

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2016
2016
Amelogenesis imperfecta (AI) is a heterogeneous group of genetic disorders affecting tooth enamel. The affected enamel can be… (More)
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2013
2013
Amelogenesis imperfecta (AI) can be either isolated or part of a larger syndrome. Junctional epidermolysis bullosa (JEB) is a… (More)
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2012
2012
Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental enamel defects without any… (More)
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2012
2012
Amelogenesis imperfecta (AI) is a group of inherited conditions featuring isolated enamel malformations. About 5% of AI cases… (More)
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2011
2011
Amelogenesis imperfecta (AI) represents hereditary conditions affecting the quality and quantity of enamel. Six genes are known… (More)
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2003
2003
Amelogenesis imperfecta (AI) is a group of inherited disorders with defective tooth enamel formation caused by various gene… (More)
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2002
2002
Amelogenesis imperfecta (AI) is currently classified into 14 distinct subtypes based on various phenotypic criteria; however, the… (More)
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2001
2001
A gene encoding the enamel protein ameloblastin (AMBN) was recently localized to a region on chromosome 4q21 containing a gene… (More)
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1991
1991
Amelogenesis imperfecta (AI) comprises a diverse group of hereditary enamel disorders that are characterized by hypoplastic and… (More)
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1988
1988
A case is presented of a 12-year-old Japanese girl with nearly complete lack of enamel in the deciduous and the permanent… (More)
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