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Clinical Genetics|August 31, 1999
Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditionsJ A Price, J T Wright, S J Walker, et al.Archives 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.Histology and Histopathology|June 7, 2003
Characterization and mRNA expression in an unusual odontogenic lesion in a patient with tricho-dento-osseous syndromeA P Dodds, S A Cox, C A Suggs, 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.Otolaryngologic Clinics of North America|February 1, 1997
Applications of molecular epidemiology to head and neck cancerT C HartCurrent Opinion in Periodontology|January 1, 1994
Genetic considerations of risk in human periodontal diseaseT C HartJournal of Dental Research|May 2, 2009
Phenotypic variation in FAM83H-associated amelogenesis imperfectaJ T Wright, S Frazier-Bowers, D Simmons, et al.Oral Diseases|January 16, 2009
Enamel defects and salivary methylmalonate in methylmalonic acidemiaC W Bassim, J T Wright, J P Guadagnini, et al.Connective Tissue Research|September 4, 2003
Relationship of phenotype and genotype in X-linked amelogenesis imperfectaJ T Wright, P S Hart, M J Aldred, et al.Pageof 25