Home > A. Molecular pathology > MSX1
MSX1
Monday 6 June 2005
Pathology
germline mutations in
- autosomal dominant hypodontia (MIM.106600)
- Witkop syndrome (tooth-and-nail syndrome) (MIM.189500)
- isolated cleft lip/palate (MIM.608874)
See also
MSXs
- MSX1
- MSX2
