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

P S Henthorn

Showing results (1-10 of 60) with videos related to

Pageof 6
Sort By:
Clinical Chemistry|December 1, 1992
Missense mutations of the tissue-nonspecific alkaline phosphatase gene in hypophosphatasiaP S Henthorn, M P Whyte
Prenatal Diagnosis|November 1, 1995
Infantile hypophosphatasia: successful prenatal assessment by testing for tissue-non-specific alkaline phosphatase isoenzyme gene mutationsP S Henthorn, M P Whyte
Progress in Clinical and Biological Research|January 1, 1985
A retrovirus-like element occurs between the 3' breakpoints of two large deletions in the human beta-globin gene clusterD L Mager, P S Henthorn
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1984
Identification of a retrovirus-like repetitive element in human DNAD L Mager, P S Henthorn
Genomics|February 1, 1990
Molecular analysis of deletions in the human beta-globin gene cluster: deletion junctions and locations of breakpointsP S Henthorn, O Smithies, D L Mager
Nucleic Acids Research|September 25, 1985
A Chinese G gamma + (A gamma delta beta)zero thalassemia deletion: comparison to other deletions in the human beta-globin gene cluster and sequence analysis of the breakpointsD L Mager, P S Henthorn, O Smithies
American Journal of Medical Genetics|December 26, 2001
Differing opinion regarding the etiology of juvenile cardiomyopathy in Portuguese water dogsM M Sleeper, P S Henthorn, E B Lankford
Biochemical Genetics|April 1, 1981
Murine liver arylsulfatase B processing influenced by region on chromosome 17W L Daniel, J E Womack, P S Henthorn
Nucleic Acids Research|February 11, 1991
A high-frequency RFLP at the human TFE3 locus on the X chromosomeJ M Puck, C C Stewart, P S Henthorn
Genomics|October 1, 1991
The gene encoding human TFE3, a transcription factor that binds the immunoglobulin heavy-chain enhancer, maps to Xp11.22P S Henthorn, C C Stewart, T Kadesch, et al.
Pageof 6

Showing results (1-10 of 60) with videos related to

Sort By:
Pageof 6
Clinical Chemistry|December 1, 1992
Missense mutations of the tissue-nonspecific alkaline phosphatase gene in hypophosphatasiaP S Henthorn, M P Whyte
Prenatal Diagnosis|November 1, 1995
Infantile hypophosphatasia: successful prenatal assessment by testing for tissue-non-specific alkaline phosphatase isoenzyme gene mutationsP S Henthorn, M P Whyte
Progress in Clinical and Biological Research|January 1, 1985
A retrovirus-like element occurs between the 3' breakpoints of two large deletions in the human beta-globin gene clusterD L Mager, P S Henthorn
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1984
Identification of a retrovirus-like repetitive element in human DNAD L Mager, P S Henthorn
Genomics|February 1, 1990
Molecular analysis of deletions in the human beta-globin gene cluster: deletion junctions and locations of breakpointsP S Henthorn, O Smithies, D L Mager
Nucleic Acids Research|September 25, 1985
A Chinese G gamma + (A gamma delta beta)zero thalassemia deletion: comparison to other deletions in the human beta-globin gene cluster and sequence analysis of the breakpointsD L Mager, P S Henthorn, O Smithies
American Journal of Medical Genetics|December 26, 2001
Differing opinion regarding the etiology of juvenile cardiomyopathy in Portuguese water dogsM M Sleeper, P S Henthorn, E B Lankford
Biochemical Genetics|April 1, 1981
Murine liver arylsulfatase B processing influenced by region on chromosome 17W L Daniel, J E Womack, P S Henthorn
Nucleic Acids Research|February 11, 1991
A high-frequency RFLP at the human TFE3 locus on the X chromosomeJ M Puck, C C Stewart, P S Henthorn
Genomics|October 1, 1991
The gene encoding human TFE3, a transcription factor that binds the immunoglobulin heavy-chain enhancer, maps to Xp11.22P S Henthorn, C C Stewart, T Kadesch, et al.
Pageof 6