Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/ejhg2014159.pdf
Reference78 articles.
1. Zhang J, Wang J, Ma Y et al: A novel splicing mutation alters DSPP transcription and leads to dentinogenesis imperfecta type II. PLoS One 2011; 6: e27982.
2. Hart PS, Hart TC : Disorders of human dentin. Cells Tissues Organs 2007; 186: 70–77.
3. Kim JW, Simmer JP : Hereditary dentin defects. J Dent Res 2007; 86: 392–399.
4. Barron MJ, McDonnell ST, Mackie I, Dixon MJ : Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia. Orphanet J Rare Dis 2008; 3: 31.
5. Witkop Jr CJ : Hereditary defects of dentin. Dent Clin North Am 1975; 19: 25–45.
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