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 P Dryja

Showing results (61-70 of 141) with videos related to

Pageof 15
Sort By:
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1996
Norrie disease. Diagnosis of a simplex case by DNA analysisE W Chynn, D S Walton, L B Hahn, et al.
Journal of Medical Genetics|December 1, 1994
Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreousP J Rosenfeld, V A McKusick, J S Amberger, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1986
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomasT P Dryja, J M Rapaport, J M Joyce, et al.
Genomics|August 1, 1994
Nonallelic heterogeneity in autosomal dominant retinitis pigmentosa with incomplete penetranceS K Kim, J L Haines, E L Berson, et al.
Gene|September 1, 1983
Retrieval of human DNA from rodent-human genomic libraries by a recombination processR L Neve, G A Bruns, T P Dryja, et al.
Investigative Ophthalmology & Visual Science|March 21, 1998
Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindnessK C Sippel, J D DeStefano, E L Berson, et al.
Investigative Ophthalmology & Visual Science|June 1, 1978
Demonstration of tyrosinase in the adult bovine uveal tract and retinal pigment epitheliumT P Dryja, M O'Neil-Dryja, J M Pawelek, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 1995
Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosaM E McLaughlin, T L Ehrhart, E L Berson, et al.
Investigative Ophthalmology & Visual Science|July 7, 1999
Frequency of mutations in the gene encoding the alpha subunit of rod cGMP-phosphodiesterase in autosomal recessive retinitis pigmentosaT P Dryja, D E Rucinski, S H Chen, et al.
Nature Genetics|June 1, 1993
Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosaM E McLaughlin, M A Sandberg, E L Berson, et al.
Pageof 15

Showing results (61-70 of 141) with videos related to

Sort By:
Pageof 15
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1996
Norrie disease. Diagnosis of a simplex case by DNA analysisE W Chynn, D S Walton, L B Hahn, et al.
Journal of Medical Genetics|December 1, 1994
Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreousP J Rosenfeld, V A McKusick, J S Amberger, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1986
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomasT P Dryja, J M Rapaport, J M Joyce, et al.
Genomics|August 1, 1994
Nonallelic heterogeneity in autosomal dominant retinitis pigmentosa with incomplete penetranceS K Kim, J L Haines, E L Berson, et al.
Gene|September 1, 1983
Retrieval of human DNA from rodent-human genomic libraries by a recombination processR L Neve, G A Bruns, T P Dryja, et al.
Investigative Ophthalmology & Visual Science|March 21, 1998
Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindnessK C Sippel, J D DeStefano, E L Berson, et al.
Investigative Ophthalmology & Visual Science|June 1, 1978
Demonstration of tyrosinase in the adult bovine uveal tract and retinal pigment epitheliumT P Dryja, M O'Neil-Dryja, J M Pawelek, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 1995
Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosaM E McLaughlin, T L Ehrhart, E L Berson, et al.
Investigative Ophthalmology & Visual Science|July 7, 1999
Frequency of mutations in the gene encoding the alpha subunit of rod cGMP-phosphodiesterase in autosomal recessive retinitis pigmentosaT P Dryja, D E Rucinski, S H Chen, et al.
Nature Genetics|June 1, 1993
Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosaM E McLaughlin, M A Sandberg, E L Berson, et al.
Pageof 15