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Amelogenesis Imperfecta, Type IB

Known as: AIH2, AMELOGENESIS IMPERFECTA, HYPOPLASTIC LOCAL, AUTOSOMAL DOMINANT, ENAMEL HYPOPLASIA, HEREDITARY LOCALIZED 
 
National Institutes of Health

Papers overview

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2015
2015
AbstractAn association of human leukocyte antigen (HLA) class II alleles with autoimmune conditions is increasingly being used… Expand
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2014
2014
There are three clinical patterns of AIH presentation: an acute pattern (rarely fulminant, particularly in AIH2) in approximately… Expand
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Review
2010
Review
2010
BACKGROUND Graft rejection and disease recurrence are well-recognized complications of liver transplantation (LT) for autoimmune… Expand
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2007
2007
Amelogenesis imperfecta is an inherited disorder affecting tooth enamel formation. We previously isolated a mouse strain with an… Expand
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Highly Cited
2005
Highly Cited
2005
Amelogenesis imperfecta (AI) is a group of commonly inherited defects of dental enamel formation, which exhibits marked genetic… Expand
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Highly Cited
2002
Highly Cited
2002
Amelogenesis imperfecta (AI) is an inherited tooth disorder affecting tooth enamel formation only. A gene for autosomal dominant… Expand
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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… Expand
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1997
1997
Amelogenesis imperfecta (AI) is a broad group of hereditary enamel defects that is characterized by a high degree of clinical… Expand
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1997
1997
Amelogenesis imperfecta (AI) is a clinically and genetically heterogeneous group of inherited enamel defects. We recently mapped… Expand
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1997
1997
The research presented in this dissertation employs methods of quantum chemistry for the search of highly energetic chemical… Expand
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