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 W Prior

Showing results (11-20 of 75) with videos related to

Pageof 8
Sort By:
The American Journal of Otology|December 10, 1997
Detection of viral DNA in vestibular ganglia tissue from patients with Menière's diseaseD B Welling, B A Miles, L Western, et al.
The Journal of Reproductive Medicine|October 1, 1991
Glycosylated hemoglobin and fructosamine. Indicators of glycemic control in pregnancies complicated by diabetes mellitusW J Watson, W N Herbert, T W Prior, et al.
Thrombosis Research|July 15, 1996
The incidence of the gene for thermolabile methylene tetrahydrofolate reductase in African AmericansP E McAndrew, J T Brandt, D K Pearl, et al.
American Journal of Clinical Pathology|July 1, 1992
Optimization of DNA extraction from formalin-fixed tissue and its clinical application in Duchenne muscular dystrophyK F Forsthoefel, A C Papp, P J Snyder, et al.
Human Genetics|October 1, 1993
Detection of an exon 53 polymorphism in the dystrophin geneT W Prior, A C Papp, P J Snyder, et al.
Muscle & Nerve|August 1, 1992
Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophyT W Prior, A C Papp, P J Snyder, et al.
Clinical Chemistry|June 1, 1989
Use of the polymerase chain reaction for simultaneous analysis of two Pst I polymorphisms linked to cystic fibrosisW E Highsmith, T R Perry, T W Prior, et al.
American Journal of Medical Genetics|October 21, 1999
Spinal muscular atrophy variant with congenital fracturesT E Kelly, K Amoroso, M Ferre, et al.
American Journal of Human Genetics|January 1, 1995
Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin productionA V Winnard, J R Mendell, T W Prior, et al.
American Journal of Clinical Pathology|March 17, 1999
Prevalence of the factor VLeiden mutation among autopsy patients with pulmonary thromboembolic disease using an improved method for factor VLeiden detectionT E Gorman, A N Arcot, P Baker, et al.
Pageof 8

Showing results (11-20 of 75) with videos related to

Sort By:
Pageof 8
The American Journal of Otology|December 10, 1997
Detection of viral DNA in vestibular ganglia tissue from patients with Menière's diseaseD B Welling, B A Miles, L Western, et al.
The Journal of Reproductive Medicine|October 1, 1991
Glycosylated hemoglobin and fructosamine. Indicators of glycemic control in pregnancies complicated by diabetes mellitusW J Watson, W N Herbert, T W Prior, et al.
Thrombosis Research|July 15, 1996
The incidence of the gene for thermolabile methylene tetrahydrofolate reductase in African AmericansP E McAndrew, J T Brandt, D K Pearl, et al.
American Journal of Clinical Pathology|July 1, 1992
Optimization of DNA extraction from formalin-fixed tissue and its clinical application in Duchenne muscular dystrophyK F Forsthoefel, A C Papp, P J Snyder, et al.
Human Genetics|October 1, 1993
Detection of an exon 53 polymorphism in the dystrophin geneT W Prior, A C Papp, P J Snyder, et al.
Muscle & Nerve|August 1, 1992
Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophyT W Prior, A C Papp, P J Snyder, et al.
Clinical Chemistry|June 1, 1989
Use of the polymerase chain reaction for simultaneous analysis of two Pst I polymorphisms linked to cystic fibrosisW E Highsmith, T R Perry, T W Prior, et al.
American Journal of Medical Genetics|October 21, 1999
Spinal muscular atrophy variant with congenital fracturesT E Kelly, K Amoroso, M Ferre, et al.
American Journal of Human Genetics|January 1, 1995
Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin productionA V Winnard, J R Mendell, T W Prior, et al.
American Journal of Clinical Pathology|March 17, 1999
Prevalence of the factor VLeiden mutation among autopsy patients with pulmonary thromboembolic disease using an improved method for factor VLeiden detectionT E Gorman, A N Arcot, P Baker, et al.
Pageof 8