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T C Hart

Showing results (51-60 of 92) with videos related to

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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 Periodontology|June 29, 2000
Genetic polymorphisms of the IL-1alpha and IL-1beta genes in African-American LJP patients and an African-American control populationS J Walker, T E Van Dyke, S Rich, et al.
Journal of Dental Research|November 15, 2000
Evidence of genetic heterogeneity for hereditary gingival fibromatosisT C Hart, D Pallos, L Bozzo, 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.
Journal of Medical Genetics|July 6, 2004
Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfectaP S Hart, T C Hart, M D Michalec, 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.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 21, 2000
An integrated physical and genetic map of the PLS locus interval on chromosome 11q14T C Hart, S J Walker, D W Bowden, 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.
Pageof 10

Showing results (51-60 of 92) with videos related to

Sort By:
Pageof 10
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 Periodontology|June 29, 2000
Genetic polymorphisms of the IL-1alpha and IL-1beta genes in African-American LJP patients and an African-American control populationS J Walker, T E Van Dyke, S Rich, et al.
Journal of Dental Research|November 15, 2000
Evidence of genetic heterogeneity for hereditary gingival fibromatosisT C Hart, D Pallos, L Bozzo, 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.
Journal of Medical Genetics|July 6, 2004
Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfectaP S Hart, T C Hart, M D Michalec, 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.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 21, 2000
An integrated physical and genetic map of the PLS locus interval on chromosome 11q14T C Hart, S J Walker, D W Bowden, 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.
Pageof 10