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

V C Sheffield

Showing results (81-90 of 153) with videos related to

Pageof 16
Sort By:
Journal of Neurodevelopmental Disorders|May 7, 2011
Novel copy number variants in children with autism and additional developmental anomaliesL K Davis, K J Meyer, D S Rudd, et al.
Human Genetics|March 7, 2008
Pax6 3' deletion results in aniridia, autism and mental retardationL K Davis, K J Meyer, D S Rudd, et al.
Human Genetics|February 1, 1994
Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21A J Cousineau, R M Lauer, M E Pierpont, et al.
Human Molecular Genetics|December 1, 1992
Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13E M Stone, A E Kimura, J C Folk, et al.
Nature Genetics|May 1, 1993
Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31V C Sheffield, E M Stone, W L Alward, et al.
Investigative Ophthalmology & Visual Science|September 28, 2000
Localization of MYOC transcripts in human eye and optic nerve by in situ hybridizationR E Swiderski, J L Ross, J H Fingert, et al.
Human Molecular Genetics|October 1, 1996
Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10S Wayne, V M Der Kaloustian, M Schloss, et al.
Nature Genetics|April 1, 1994
Integrated human genome-wide maps constructed using the CEPH reference panelK H Buetow, J L Weber, S Ludwigsen, et al.
Human Molecular Genetics|April 1, 1997
Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase geneA Nystuen, H Costeff, O N Elpeleg, et al.
Molecular Vision|April 26, 2001
Optimal procedure for extracting RNA from human ocular tissues and expression profiling of the congenital glaucoma gene FOXC1 using quantitative RT-PCRW H Wang, L G McNatt, A R Shepard, et al.
Pageof 16

Showing results (81-90 of 153) with videos related to

Sort By:
Pageof 16
Journal of Neurodevelopmental Disorders|May 7, 2011
Novel copy number variants in children with autism and additional developmental anomaliesL K Davis, K J Meyer, D S Rudd, et al.
Human Genetics|March 7, 2008
Pax6 3' deletion results in aniridia, autism and mental retardationL K Davis, K J Meyer, D S Rudd, et al.
Human Genetics|February 1, 1994
Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21A J Cousineau, R M Lauer, M E Pierpont, et al.
Human Molecular Genetics|December 1, 1992
Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13E M Stone, A E Kimura, J C Folk, et al.
Nature Genetics|May 1, 1993
Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31V C Sheffield, E M Stone, W L Alward, et al.
Investigative Ophthalmology & Visual Science|September 28, 2000
Localization of MYOC transcripts in human eye and optic nerve by in situ hybridizationR E Swiderski, J L Ross, J H Fingert, et al.
Human Molecular Genetics|October 1, 1996
Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10S Wayne, V M Der Kaloustian, M Schloss, et al.
Nature Genetics|April 1, 1994
Integrated human genome-wide maps constructed using the CEPH reference panelK H Buetow, J L Weber, S Ludwigsen, et al.
Human Molecular Genetics|April 1, 1997
Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase geneA Nystuen, H Costeff, O N Elpeleg, et al.
Molecular Vision|April 26, 2001
Optimal procedure for extracting RNA from human ocular tissues and expression profiling of the congenital glaucoma gene FOXC1 using quantitative RT-PCRW H Wang, L G McNatt, A R Shepard, et al.
Pageof 16