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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

Semantic Scholar uses AI to extract papers important to this topic.
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
Watch a video presentation of this article 
Review
2010
Review
2010
Background: Graft rejection and disease recurrence are well-recognized complications of liver transplantation (LT) for autoimmune… Expand
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
Highly Cited
1997
Highly Cited
1997
Amelogenesis imperfecta (AI) is a broad group of hereditary enamel defects that is characterized by a high degree of clinical… Expand
1997
1997
Amelogenesis imperfecta (AI) is a clinically and genetically heterogeneous group of inherited enamel defects. We recently mapped… Expand
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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