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T C Hart

Showing results (41-50 of 92) with videos related to

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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.
Calcified Tissue International|January 11, 2003
Aquaporin expression in developing human teeth and selected orofacial tissuesW Wang, P S Hart, N P Piesco, et al.
Molecular Genetics and Metabolism|June 27, 2002
Identification of a novel cathepsin C mutation (p.W185X) in a Brazilian kindred with Papillon-Lefèvre syndromeP S Hart, D Pallos, Y Zhang, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Assignment of the sodium-dependent dicarboxylate transporter gene (SLC13A2 alias NaDC-1) to human chromosome region 17p11.1-->q11.1 by radiation hybrid mapping and fluorescence in situ hybridizationS S Mann, T C Hart, M J Pettenati, et al.
American Journal of Human Genetics|June 13, 1998
Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21T C Hart, D Pallos, D W Bowden, et al.
Cytogenetics and Cell Genetics|August 31, 2000
Assignment of PDZ domain-containing protein GIPC gene (C19orf3) to human chromosome band 19p13.1 by in situ hybridization and radiation hybrid mappingC Von Kap-Herr, G Kandala, S S Mann, et al.
Genomics|July 1, 1994
Assignment of the human diacylglycerol kinase gene (DAGK) to 12q13.3 using fluorescence in situ hybridization analysisT C Hart, J Zhou, C Champagne, et al.
Archives of Oral Biology|March 3, 2005
Mutans streptococci in preschool twinsP M A Corby, W A Bretz, T C Hart, et al.
Journal of Periodontology|December 1, 1991
No female preponderance in juvenile periodontitis after correction for ascertainment biasT C Hart, M L Marazita, H A Schenkein, et al.
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.
Pageof 10

Showing results (41-50 of 92) with videos related to

Sort By:
Pageof 10
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.
Calcified Tissue International|January 11, 2003
Aquaporin expression in developing human teeth and selected orofacial tissuesW Wang, P S Hart, N P Piesco, et al.
Molecular Genetics and Metabolism|June 27, 2002
Identification of a novel cathepsin C mutation (p.W185X) in a Brazilian kindred with Papillon-Lefèvre syndromeP S Hart, D Pallos, Y Zhang, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Assignment of the sodium-dependent dicarboxylate transporter gene (SLC13A2 alias NaDC-1) to human chromosome region 17p11.1-->q11.1 by radiation hybrid mapping and fluorescence in situ hybridizationS S Mann, T C Hart, M J Pettenati, et al.
American Journal of Human Genetics|June 13, 1998
Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21T C Hart, D Pallos, D W Bowden, et al.
Cytogenetics and Cell Genetics|August 31, 2000
Assignment of PDZ domain-containing protein GIPC gene (C19orf3) to human chromosome band 19p13.1 by in situ hybridization and radiation hybrid mappingC Von Kap-Herr, G Kandala, S S Mann, et al.
Genomics|July 1, 1994
Assignment of the human diacylglycerol kinase gene (DAGK) to 12q13.3 using fluorescence in situ hybridization analysisT C Hart, J Zhou, C Champagne, et al.
Archives of Oral Biology|March 3, 2005
Mutans streptococci in preschool twinsP M A Corby, W A Bretz, T C Hart, et al.
Journal of Periodontology|December 1, 1991
No female preponderance in juvenile periodontitis after correction for ascertainment biasT C Hart, M L Marazita, H A Schenkein, et al.
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.
Pageof 10