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Archives of Oral Biology|April 2, 2002
A nomenclature for X-linked amelogenesis imperfectaP S Hart, T C Hart, J P Simmer, et al.Journal of Dental Research|November 26, 2008
Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfectaD A McKnight, J P Simmer, P S Hart, et al.Archives of Oral Biology|June 28, 2003
Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclatureP S Hart, M D Michalec, W K Seow, et al.Orthodontics & Craniofacial Research|July 25, 2009
Genetic studies of craniofacial anomalies: clinical implications and applicationsT C Hart, P S HartJournal of Dental Education|June 12, 2002
The genome projects: implications for dental practice and educationJ T Wright, T C HartArchives of Oral Biology|April 2, 2002
Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutationsP S Hart, M J Aldred, P J M Crawford, et al.Journal of Dental Research|September 27, 2000
Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutationD B Ravassipour, P S Hart, T C Hart, et al.Archives of Oral Biology|April 5, 2001
Novel COL1A1 mutation (G559C) [correction of G599C] associated with mild osteogenesis imperfecta and dentinogenesis imperfectaD Pallos, P S Hart, J R Cortelli, et al.Journal of Dental Research|May 2, 2009
Phenotypic variation in FAM83H-associated amelogenesis imperfectaJ T Wright, S Frazier-Bowers, D Simmons, et al.Critical Reviews in Oral Biology and Medicine : an Official Publication of the American Association of Oral Biologists|February 22, 2000
The impact of molecular genetics on oral health paradigmsT C Hart, M L Marazita, J T WrightPageof 36