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 (21-30 of 75) with videos related to

Pageof 8
Sort By:
The American Journal of Otology|September 1, 1994
Detection of viral DNA in endolymphatic sac tissue from Menière's disease patientsD B Welling, R L Daniels, J Brainard, et al.
Clinical Chemistry|April 1, 1989
Use of DNA probes in detecting carriers of Duchenne muscular dystrophy: selected case studiesT W Prior, P A Blasco, J L Dove, et al.
Clinical Chemistry|March 11, 1990
Molecular probe protocol for determining carrier status in Duchenne and Becker muscular dystrophiesT W Prior, K J Friedman, W E Highsmith, et al.
Human Genetics|August 1, 1992
A HindIII/BglII dystrophin gene polymorphism in the African-American populationT W Prior, A C Papp, P J Snyder, et al.
Human Mutation|January 11, 2000
Polymorphisms in a pseudogene highly homologous to PMS2R B Chadwick, J E Meek, T W Prior, et al.
Clinical Chemistry|April 1, 1990
Cystic fibrosis deletion mutation detected by PCR-mediated site-directed mutagenesisK J Friedman, W E Highsmith, T W Prior, et al.
Human Pathology|May 31, 2001
Increased D allele frequency of the angiotensin-converting enzyme gene in pulmonary fibrosisC D Morrison, A C Papp, A Q Hejmanowski, et al.
Neurology|April 1, 1993
Kennedy's disease: a clinicopathologic correlation with mutations in the androgen receptor geneA A Amato, T W Prior, R J Barohn, et al.
Neurology|February 7, 2007
Preclinical validation of a multiplex real-time assay to quantify SMN mRNA in patients with SMAL R Simard, M-C Bélanger, S Morissette, et al.
Clinical Chemistry|October 1, 1996
Southern transfer protocol for confirmation of Huntington diseaseM Guida, R G Fenwick, A C Papp, et al.
Pageof 8

Showing results (21-30 of 75) with videos related to

Sort By:
Pageof 8
The American Journal of Otology|September 1, 1994
Detection of viral DNA in endolymphatic sac tissue from Menière's disease patientsD B Welling, R L Daniels, J Brainard, et al.
Clinical Chemistry|April 1, 1989
Use of DNA probes in detecting carriers of Duchenne muscular dystrophy: selected case studiesT W Prior, P A Blasco, J L Dove, et al.
Clinical Chemistry|March 11, 1990
Molecular probe protocol for determining carrier status in Duchenne and Becker muscular dystrophiesT W Prior, K J Friedman, W E Highsmith, et al.
Human Genetics|August 1, 1992
A HindIII/BglII dystrophin gene polymorphism in the African-American populationT W Prior, A C Papp, P J Snyder, et al.
Human Mutation|January 11, 2000
Polymorphisms in a pseudogene highly homologous to PMS2R B Chadwick, J E Meek, T W Prior, et al.
Clinical Chemistry|April 1, 1990
Cystic fibrosis deletion mutation detected by PCR-mediated site-directed mutagenesisK J Friedman, W E Highsmith, T W Prior, et al.
Human Pathology|May 31, 2001
Increased D allele frequency of the angiotensin-converting enzyme gene in pulmonary fibrosisC D Morrison, A C Papp, A Q Hejmanowski, et al.
Neurology|April 1, 1993
Kennedy's disease: a clinicopathologic correlation with mutations in the androgen receptor geneA A Amato, T W Prior, R J Barohn, et al.
Neurology|February 7, 2007
Preclinical validation of a multiplex real-time assay to quantify SMN mRNA in patients with SMAL R Simard, M-C Bélanger, S Morissette, et al.
Clinical Chemistry|October 1, 1996
Southern transfer protocol for confirmation of Huntington diseaseM Guida, R G Fenwick, A C Papp, et al.
Pageof 8