Ectodermal Dysplasia: A Case Report
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-10005-1124
Reference8 articles.
1. 1. Pinheiro M, Freire-Maia N. Ectodermal dysplasia: A clinical classification and a casual review. Am J Med Genet Nov 1, 1994;53(2):153-62.
2. 2. Smith FJ, Jonkman MF, Van Goor, et al. A mutation in human keratin K6b produces a phenocopy of the K17 disorders pachyonychia type 2. Hum Mol Genet Jul 1998;7(7):1143-48.
3. 3. Mc Lean WH, et al. Keratine 16 and keratine 17 mutations causes pachyonychia congenital. Nat Genet Mar 1995;9(3): 273-78.
4. 4. Boden PE, Haley JL, et al. Mutation of a type II keratine gene (K6a) in pachyonychia congenital. Nat Genet Jul 1995;10(3): 363-65.
5. 5. Kere J, Srivastava AK, Montonen O, et al. X-linked anhidrotic (hypohydrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet Aug 1996;13(4):409-16.
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