NovelFAM83Hmutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2008.01112.x/fullpdf
Reference11 articles.
1. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited, problems in classification;Witkop;J Oral Pathol,1988
2. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta;Wright;Connect Tissue Res,2003
3. Identification of the enamelin mutation (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature;Hart;Arch Oral Biol,2003
4. Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta;Hart;J Med Genet,2004
5. MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta;Kim;J Med Genet,2005
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