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

S Harper

Showing results (571-580 of 1,225) with videos related to

Pageof 123
Sort By:
Clinical Genetics|September 11, 2002
Developing a quality scoring system for epidemiological surveys of genetic disordersL N Al-Jader, R G Newcombe, S Hayes, et al.
Vaccine|July 18, 2001
Response to HBV vaccine in relation to vaccine dose and anti-HCV positivity: a New South Wales correctional facilities' studyN Awofeso, M Levy, S Harper, et al.
Biochemical Society Transactions|November 1, 1995
Characterising the Huntington's disease gene productJ Wood, J C MacMillan, P Thomas, et al.
Leukemia & Lymphoma|October 10, 2025
Treatment-emergent peripheral neuropathy associated with bortezomib-based frontline regimens for multiple myelomaCarlyn Tan, Jennifer S Harper, Santosh Gautam, et al.
Chronic Diseases and Injuries in Canada|July 4, 2014
Modelling preventive effectiveness to estimate the equity tipping point: at what coverage can individual preventive interventions reduce socioeconomic disparities in diabetes risk?D G Manuel, T H Ho, S Harper, et al.
Pharmaceutics|April 3, 2021
The Combination of Tissue-Engineered Blood Vessel Constructs and Parallel Flow Chamber Provides a Potential Alternative to In Vivo Drug Testing ModelsWanjiku Njoroge, Andrea C Hernández Hernández, Faiza Idris Musa, et al.
Cytogenetics and Cell Genetics|January 1, 1986
Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybridsJ D Brook, D J Shaw, N S Thomas, et al.
Journal of Medical Genetics|June 1, 1985
Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosomeC S Brown, P L Pearson, N S Thomas, et al.
American Journal of Medical Genetics|September 1, 1983
Carrier detection in Hunter syndromeI M Archer, I D Young, D W Rees, et al.
Journal of Medical Genetics|June 1, 1997
Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHDM Upadhyaya, J Maynard, M T Rogers, et al.
Pageof 123

Showing results (571-580 of 1,225) with videos related to

Sort By:
Pageof 123
Clinical Genetics|September 11, 2002
Developing a quality scoring system for epidemiological surveys of genetic disordersL N Al-Jader, R G Newcombe, S Hayes, et al.
Vaccine|July 18, 2001
Response to HBV vaccine in relation to vaccine dose and anti-HCV positivity: a New South Wales correctional facilities' studyN Awofeso, M Levy, S Harper, et al.
Biochemical Society Transactions|November 1, 1995
Characterising the Huntington's disease gene productJ Wood, J C MacMillan, P Thomas, et al.
Leukemia & Lymphoma|October 10, 2025
Treatment-emergent peripheral neuropathy associated with bortezomib-based frontline regimens for multiple myelomaCarlyn Tan, Jennifer S Harper, Santosh Gautam, et al.
Chronic Diseases and Injuries in Canada|July 4, 2014
Modelling preventive effectiveness to estimate the equity tipping point: at what coverage can individual preventive interventions reduce socioeconomic disparities in diabetes risk?D G Manuel, T H Ho, S Harper, et al.
Pharmaceutics|April 3, 2021
The Combination of Tissue-Engineered Blood Vessel Constructs and Parallel Flow Chamber Provides a Potential Alternative to In Vivo Drug Testing ModelsWanjiku Njoroge, Andrea C Hernández Hernández, Faiza Idris Musa, et al.
Cytogenetics and Cell Genetics|January 1, 1986
Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybridsJ D Brook, D J Shaw, N S Thomas, et al.
Journal of Medical Genetics|June 1, 1985
Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosomeC S Brown, P L Pearson, N S Thomas, et al.
American Journal of Medical Genetics|September 1, 1983
Carrier detection in Hunter syndromeI M Archer, I D Young, D W Rees, et al.
Journal of Medical Genetics|June 1, 1997
Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHDM Upadhyaya, J Maynard, M T Rogers, et al.
Pageof 123