Management of Dentinogenesis Imperfecta: A Report of Two Cases
Author:
Publisher
Jaypee Brothers Medical Publishing
Subject
Periodontics,Oral Surgery,Pediatrics, Perinatology and Child Health,Orthodontics
Link
https://www.ijcpd.com/doi/pdf/10.5005/jp-journals-10005-1681
Reference10 articles.
1. 1. Kim JW, Simmer JP. Hereditary dentin defects. J Dent Res 2007;86(5):392–399. DOI: 10.1177/154405910708600502.
2. 2. Tahmassebi JF, Day PF, et al. Paediatric dentistry in the new millennium: dental anomalies in children. Dent Update 2003;30: 534–540. DOI: 10.12968/denu.2003.30.10.534.
3. 3. Witkop CJ. Genetics and dentistry. Eugen Quart 1958;5:15–21. DOI: 10.1080/19485565.1958.9987342.
4. 4. Holappa H, Nieminen P, et al. Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II. Eur J Oral Sci 2006;114:381–384. DOI: 10.1111/j.1600-0722.2006.00391.x.
5. 5. Shafer WG, Hine MK, et al. A textbook of Oral Pathology. 4th ed., Philadelphia: WB Saunders Co; 1983. p. 37.
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