Showing results (61-70 of 109) with videos related to
Sort By:
Pageof 11
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.Journal of Periodontal Research|January 1, 1997
Genetic studies of syndromes with severe periodontitis and palmoplantar hyperkeratosisT C Hart, A Stabholz, J Meyle, et al.Oral Diseases|January 5, 2008
Novel intraoral phenotypes in hyperimmunoglobulin-E syndromeD L Domingo, A F Freeman, J Davis, et al.Journal of Medical Genetics|October 3, 1999
Genetic heterogeneity of gingival fibromatosis on chromosome 2pV Shashi, D Pallos, M J Pettenati, et al.Science (New York, N.Y.)|November 8, 1985
Energy extraction and use in a nomadic pastoral ecosystemM B Coughenour, J E Ellis, D M Swift, et al.American Journal of Medical Genetics|September 19, 1998
Sublocalization of the Papillon-Lefevre syndrome locus on 11q14-q21T C Hart, D W Bowden, K A Ghaffar, 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.Oral Diseases|March 18, 2010
Craniofacial and dental findings in cystinosisC W Bassim, P Gautam, D L Domingo, 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.Pageof 11