Journal of Evidence-Based Dental Practice
Volume 5, Issue 3 , Pages 160-161 , September 2005

DNA sequence variations in the genes MSX1 and TGFA may lead to developmentally missing teeth

References 

  1. De Muynck S, Schollen E, Matthijs G, Verdonck A, Devriendt K, Carels C. A novel MSX1 mutation in hypodontia. Am J Med Genet A. 2004;128(4):401–403
  2. Slayton RL, Williams L, Murray JC, Wheeler JJ, Lidral AC, Nishimura CJ. Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region. Cleft Palate Craniofac J. 2003;40(3):274–279
  3. Lidral AC, Reising BC. The role of MSX1 in human tooth agenesis. J Dent Res. 2002;81(4):274–278
  4. Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE. A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nat Genet. 1996;13(4):417–421

PII: S1532-3382(05)00103-X

doi: 10.1016/j.jebdp.2005.06.015

Journal of Evidence-Based Dental Practice
Volume 5, Issue 3 , Pages 160-161 , September 2005

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