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Amelogenesis Imperfecta, Type III

Known as: Amelogenesis Imperfecta, Hypomineralization Type, AI3, Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Dominant 
 
National Institutes of Health

Papers overview

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2011
2011
Mutations in a family with sequence similarity 83 member H (FAM83H) cause autosomal-dominant hypocalcification amelogenesis… Expand
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Highly Cited
2009
Highly Cited
2009
The combination of recessively inherited cone-rod dystrophy (CRD) and amelogenesis imperfecta (AI) was first reported by Jalili… Expand
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2009
2009
FAM83H gene mutations are associated with autosomal-dominant hypocalcified amelogenesis imperfecta (ADHCAI), which is typically… Expand
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2009
2009
Background: Nonsense mutations in FAM83H are a recently described underlying cause of autosomal dominant (AD) hypocalcified… Expand
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2006
2006
OBJECTIVE The aim of this study was to evaluate the effect of the treatment of sodium hypochlorite (NaOCl) after acid… Expand
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2004
2004
Abstract The repellents N,N-diethyl-3-methylbenzamide (deet) and racemic 2-methylpiperidinyl-3-cyclohexene-1-carboxamide (AI3… Expand
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2004
2004
Abstract The insect repellents N,N-diethyl-3-methylbenzamide (Deet) and the racemate and 1S,2′S stereoisomer of 2… Expand
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Highly Cited
2000
Highly Cited
2000
To determine the prevalence of nonfluoride enamel hypomineralization in the permanent first molars, we examined 488 7– to 13–year… Expand
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1996
1996
A field evaluation of the repellents N,N-diethyl-3-methylbenzamide (deet) and 1-(3-cyclohexen-1-yl-carbonyl)-2-methylpiperidine… Expand
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Highly Cited
1994
Highly Cited
1994
Bonding composite resin to enamel of teeth affected by amelogenesis imperfecta (AI) is often problematic, especially in cases… Expand
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