Amelogenesis imperfecta: the orthodontic perspective
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Dentistry
Link
http://www.nature.com/articles/sj.bdj.2012.415.pdf
Reference28 articles.
1. Witkop C J Jr . Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. J Oral Pathol 1988; 17: 547–553.
2. Yip H K, Smales R J . Oral rehabilitation of young adults with amelogenesis imperfecta. Int J Prosthodont 2003; 16: 345–349.
3. Kida M, Ariga T, Shirakawa T, Oquchi H, Sakiyama Y . Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary. J Dent Res 2002; 81: 738–742.
4. Dong J, Gu T T, Simmons D, MacDougall M . Enamelin maps to human chromosome 4q21 within the autosomal dominant amelogenesis imperfecta locus. Eur J Oral Sci 2000; 108: 353–358.
5. MacDougall M, Simmons D, Gu T T et al. Cloning, characterization and immunolocalization of human ameloblastin. Eur J Oral Sci 2000; 108: 303–310.
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