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 (31-40 of 153) with videos related to

Pageof 16
Sort By:
American Journal of Human Genetics|October 1, 1991
Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, G A Fishman, J S Beck, et al.
American Journal of Human Genetics|June 23, 1998
Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43R Parvari, E Hershkovitz, A Kanis, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1992
Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosaG A Fishman, E M Stone, V C Sheffield, et al.
Genomics|May 1, 1993
The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutionsV C Sheffield, J S Beck, A E Kwitek, et al.
Circulation|November 15, 1995
Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defectsM M Zittergruen, J C Murray, R M Lauer, et al.
Anticancer Research|November 1, 1996
Focal microsatellite mutations in relatives with prostatic adenocarcinomaA H Wille, R B Terrell, J C Cheville, et al.
Journal of Glaucoma|August 1, 1996
Molecular genetics of glaucoma: current statusW L Alward, A T Johnson, D Y Nishimura, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 21, 1997
X-linked retinitis pigmentosa associated with a 2-base pair insertion in codon 99 of the RP3 gene RPGRR G Weleber, N S Butler, W H Murphey, et al.
Nature|January 9, 1998
Connexin mutations and hearing lossD A Scott, M L Kraft, E M Stone, et al.
American Journal of Human Genetics|January 1, 1994
Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1B E Nichols, R Bascom, M Litt, et al.
Pageof 16

Showing results (31-40 of 153) with videos related to

Sort By:
Pageof 16
American Journal of Human Genetics|October 1, 1991
Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, G A Fishman, J S Beck, et al.
American Journal of Human Genetics|June 23, 1998
Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43R Parvari, E Hershkovitz, A Kanis, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1992
Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosaG A Fishman, E M Stone, V C Sheffield, et al.
Genomics|May 1, 1993
The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutionsV C Sheffield, J S Beck, A E Kwitek, et al.
Circulation|November 15, 1995
Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defectsM M Zittergruen, J C Murray, R M Lauer, et al.
Anticancer Research|November 1, 1996
Focal microsatellite mutations in relatives with prostatic adenocarcinomaA H Wille, R B Terrell, J C Cheville, et al.
Journal of Glaucoma|August 1, 1996
Molecular genetics of glaucoma: current statusW L Alward, A T Johnson, D Y Nishimura, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 21, 1997
X-linked retinitis pigmentosa associated with a 2-base pair insertion in codon 99 of the RP3 gene RPGRR G Weleber, N S Butler, W H Murphey, et al.
Nature|January 9, 1998
Connexin mutations and hearing lossD A Scott, M L Kraft, E M Stone, et al.
American Journal of Human Genetics|January 1, 1994
Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1B E Nichols, R Bascom, M Litt, et al.
Pageof 16