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T C Hart

Showing results (81-90 of 92) with videos related to

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Journal of Medical Genetics|February 7, 2001
Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patientsY Zhang, T Lundgren, S Renvert, et al.
Oral Diseases|February 25, 2009
Hutchinson-Gilford progeria syndrome: oral and craniofacial phenotypesD L Domingo, M I Trujillo, S E Council, et al.
Journal of Dental Research|October 26, 2005
Longitudinal analysis of heritability for dental caries traitsW A Bretz, P M Corby, N J Schork, et al.
Genes and Immunity|February 22, 2003
Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patientsY Zhang, R Syed, C Uygar, et al.
Journal of Medical Genetics|December 10, 2002
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathyT C Hart, M C Gorry, P S Hart, et al.
Journal of Medical Genetics|February 9, 2000
Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin CT C Hart, P S Hart, M D Michalec, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 5, 2008
A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic featuresC E Dumitrescu, M H Kelly, A Khosravi, et al.
European Archives of Paediatric Dentistry : Official Journal of the European Academy of Paediatric Dentistry|March 11, 2008
Inheritance of occlusal topography: a twin studyC-Y Su, P M Corby, M A Elliot, et al.
Journal of Dental Research|June 1, 2000
Cloning human enamelin cDNA, chromosomal localization, and analysis of expression during tooth developmentC C Hu, T C Hart, B R Dupont, et al.
Journal of Clinical Microbiology|November 8, 2005
Microbial risk indicators of early childhood cariesP M Corby, J Lyons-Weiler, W A Bretz, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|February 7, 2001
Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patientsY Zhang, T Lundgren, S Renvert, et al.
Oral Diseases|February 25, 2009
Hutchinson-Gilford progeria syndrome: oral and craniofacial phenotypesD L Domingo, M I Trujillo, S E Council, et al.
Journal of Dental Research|October 26, 2005
Longitudinal analysis of heritability for dental caries traitsW A Bretz, P M Corby, N J Schork, et al.
Genes and Immunity|February 22, 2003
Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patientsY Zhang, R Syed, C Uygar, et al.
Journal of Medical Genetics|December 10, 2002
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathyT C Hart, M C Gorry, P S Hart, et al.
Journal of Medical Genetics|February 9, 2000
Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin CT C Hart, P S Hart, M D Michalec, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 5, 2008
A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic featuresC E Dumitrescu, M H Kelly, A Khosravi, et al.
European Archives of Paediatric Dentistry : Official Journal of the European Academy of Paediatric Dentistry|March 11, 2008
Inheritance of occlusal topography: a twin studyC-Y Su, P M Corby, M A Elliot, et al.
Journal of Dental Research|June 1, 2000
Cloning human enamelin cDNA, chromosomal localization, and analysis of expression during tooth developmentC C Hu, T C Hart, B R Dupont, et al.
Journal of Clinical Microbiology|November 8, 2005
Microbial risk indicators of early childhood cariesP M Corby, J Lyons-Weiler, W A Bretz, et al.
Pageof 10