Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

T C Hart

Showing results (61-70 of 92) with videos related to

Pageof 10
Sort By:
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.
Cytogenetics and Cell Genetics|June 14, 2002
Localization, genomic organization, and alternative transcription of a novel human SAM-dependent methyltransferase gene on chromosome 2p22-->p21Y Zhang, M C Gorry, P S Hart, et al.
Journal of Dental Research|October 26, 2005
MMP20 active-site mutation in hypomaturation amelogenesis imperfectaD Ozdemir, P S Hart, O H Ryu, et al.
Genomics|March 3, 1999
Cytogenetic assignment and physical mapping of the human DGKE gene to chromosome 17q22T C Hart, J A Price, P L Bobby, 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.
Human Mutation|July 12, 2002
Biochemical and mutational analyses of the cathepsin c gene (CTSC) in three North American families with Papillon Lefèvre syndromeY Zhang, P S Hart, A J Moretti, et al.
Pageof 10

Showing results (61-70 of 92) with videos related to

Sort By:
Pageof 10
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.
Cytogenetics and Cell Genetics|June 14, 2002
Localization, genomic organization, and alternative transcription of a novel human SAM-dependent methyltransferase gene on chromosome 2p22-->p21Y Zhang, M C Gorry, P S Hart, et al.
Journal of Dental Research|October 26, 2005
MMP20 active-site mutation in hypomaturation amelogenesis imperfectaD Ozdemir, P S Hart, O H Ryu, et al.
Genomics|March 3, 1999
Cytogenetic assignment and physical mapping of the human DGKE gene to chromosome 17q22T C Hart, J A Price, P L Bobby, 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.
Human Mutation|July 12, 2002
Biochemical and mutational analyses of the cathepsin c gene (CTSC) in three North American families with Papillon Lefèvre syndromeY Zhang, P S Hart, A J Moretti, et al.
Pageof 10