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

W G Pearce

Showing results (31-40 of 52) with videos related to

Pageof 6
Sort By:
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|October 1, 1990
Recession of the superior oblique tendon in A-pattern strabismusG T Drummond, W G Pearce, W F Astle
Genomics|February 1, 1992
Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7N T Bech-Hansen, B J Moore, W G Pearce
Canadian Medical Association Journal|June 21, 1975
Conjunctival papillomas in norther Canadian nativesW G Pearce, S Nigam, B Mielke, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|July 20, 2000
Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1FK M Boycott, W G Pearce, N T Bech-Hansen
American Journal of Human Genetics|September 1, 1995
Mutation of the PAX6 gene in patients with autosomal dominant keratitisF Mirzayans, W G Pearce, I M MacDonald, et al.
Ophthalmic Genetics|July 27, 1999
Histopathology and molecular basis of iridogoniodysgenesis syndromeW G Pearce, B C Mielke, S C Kulak, et al.
American Journal of Human Genetics|October 27, 1997
Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25D B Gould, A J Mears, W G Pearce, et al.
Ophthalmology|November 1, 1996
Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinctM A Walter, F Mirzayans, A J Mears, et al.
Human Molecular Genetics|June 9, 1998
Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndromeS C Kulak, K Kozlowski, E V Semina, et al.
American Journal of Human Genetics|July 1, 1997
Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanningF Mirzayans, A J Mears, S W Guo, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|October 1, 1990
Recession of the superior oblique tendon in A-pattern strabismusG T Drummond, W G Pearce, W F Astle
Genomics|February 1, 1992
Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7N T Bech-Hansen, B J Moore, W G Pearce
Canadian Medical Association Journal|June 21, 1975
Conjunctival papillomas in norther Canadian nativesW G Pearce, S Nigam, B Mielke, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|July 20, 2000
Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1FK M Boycott, W G Pearce, N T Bech-Hansen
American Journal of Human Genetics|September 1, 1995
Mutation of the PAX6 gene in patients with autosomal dominant keratitisF Mirzayans, W G Pearce, I M MacDonald, et al.
Ophthalmic Genetics|July 27, 1999
Histopathology and molecular basis of iridogoniodysgenesis syndromeW G Pearce, B C Mielke, S C Kulak, et al.
American Journal of Human Genetics|October 27, 1997
Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25D B Gould, A J Mears, W G Pearce, et al.
Ophthalmology|November 1, 1996
Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinctM A Walter, F Mirzayans, A J Mears, et al.
Human Molecular Genetics|June 9, 1998
Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndromeS C Kulak, K Kozlowski, E V Semina, et al.
American Journal of Human Genetics|July 1, 1997
Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanningF Mirzayans, A J Mears, S W Guo, et al.
Pageof 6