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Journal of Dental Research
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Letter to the Editor

Sinikka Pirinen

Department of Pedodontics and Orthodontics Institute of Dentistry P.O. Box 41 00014 University of Helsinki Finland

REFERENCES

  • Arte S., Nieminen P., Pirinen S., Thesleff I., Peltonen L. (1996). Gene defect in hypodontia: Exclusion of EGF, EGFR, and FGF-3 as candidate genes. J Dent Res 75:1346-1352.
  • Isotupa K., Laine T. (1972). Myohainen viisaudenhampaan kehittyminen. Suom Hammaslääk toim 68:172.
  • Kere J., Srivastava AK, Montonen 0, Zonana J., Thomas N., Ferguson B., et al. (1996). X-linked anhidrotic (hypohidrotic] ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nature Genet 13:409-416.[CrossRef][Medline] [Order article via Infotrieve]
  • Nieminen P., Arte S., Pirinen S., Peltonen L., Thesleff I. (1995). Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes. Hum Genet 96:305-308.[Medline] [Order article via Infotrieve]
  • Thesleff I. (1996). Two genes for missing teeth (news & views). Nature Genet 13:379-380.[CrossRef][Medline] [Order article via Infotrieve]
  • Vastardis H., Karimbux N., Guthua SW, Seidman JG, Seidman CE (1996). A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nature Genet 13:417-421.[CrossRef][Medline] [Order article via Infotrieve]

Journal of Dental Research, Vol. 76, No. 3, 728-729 (1997)
DOI: 10.1177/00220345970760030201
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A. Becker
Letter to the Editor
Journal of Dental Research, September 1, 1997; 76(9): 1526 - 1526.
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This Article
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