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 F Astle

Showing results (11-20 of 16) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 16 results.
Investigative Ophthalmology & Visual Science|April 16, 1998
Anomalies of motion perception in infantile esotropiaS Fawcett, J E Raymond, W F Astle, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 1, 1990
Juvenile xanthogranuloma of the corneoscleral limbusJ R Lewis, G T Drummond, B W Mielke, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|December 23, 2008
Visual development in infants: visual complications of periocular haemangiomasR C Frank, B J Cowan, A R Harrop, et al.
Human Molecular Genetics|February 3, 2000
Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locusB A Bejjani, D W Stockton, R A Lewis, et al.
Journal of Glaucoma|December 1, 1996
A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucomaK L Anderson, R A Lewis, B A Bejjani, et al.
American Journal of Human Genetics|April 16, 1998
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi ArabiaB A Bejjani, R A Lewis, K F Tomey, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Investigative Ophthalmology & Visual Science|April 16, 1998
Anomalies of motion perception in infantile esotropiaS Fawcett, J E Raymond, W F Astle, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 1, 1990
Juvenile xanthogranuloma of the corneoscleral limbusJ R Lewis, G T Drummond, B W Mielke, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|December 23, 2008
Visual development in infants: visual complications of periocular haemangiomasR C Frank, B J Cowan, A R Harrop, et al.
Human Molecular Genetics|February 3, 2000
Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locusB A Bejjani, D W Stockton, R A Lewis, et al.
Journal of Glaucoma|December 1, 1996
A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucomaK L Anderson, R A Lewis, B A Bejjani, et al.
American Journal of Human Genetics|April 16, 1998
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi ArabiaB A Bejjani, R A Lewis, K F Tomey, et al.
Pageof 2