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 Res75:1346-1352.
2.
Isotupa K., Laine T. (1972). Myohainen viisaudenhampaan kehittyminen. Suom Hammaslääk toim68:172.
3.
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 Genet13:409-416.
4.
Nieminen P., Arte S., Pirinen S., Peltonen L., Thesleff I. (1995). Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes. Hum Genet96:305-308.
5.
Thesleff I. (1996). Two genes for missing teeth (news & views) . Nature Genet13:379-380.
6.
Vastardis H., Karimbux N., Guthua SW, Seidman JG, Seidman CE (1996). A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nature Genet13:417-421.
