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Bronwyn Bateman

Showing results (11-20 of 17) with videos related to

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Ophthalmology|January 20, 2007
Gene conversion mutation in crystallin, beta-B2 (CRYBB2) in a Chilean family with autosomal dominant cataractJ Bronwyn Bateman, Fernando R Barria von-Bischhoffshaunsen, Leslie Richter, et al.
JAMA Ophthalmology|June 15, 2013
Distinct ocular expression in infants and children with Down syndrome in Cairo, Egypt: myopia and heart diseaseHanan H Afifi, Amira A Abdel Azeem, Hala T El-Bassyouni, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 13, 2002
Infantile cataract in the collaborative perinatal project: prevalence and risk factorsJohn Paul SanGiovanni, Emily Y Chew, George F Reed, et al.
American Journal of Medical Genetics. Part A|February 28, 2008
Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA)Leslie Richter, Pamela Flodman, Fernando Barria von-Bischhoffshausen, et al.
Investigative Ophthalmology & Visual Science|August 1, 2006
A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genesJ Bronwyn Bateman, Leslie Richter, Pamela Flodman, et al.
American Journal of Ophthalmology|March 28, 2006
Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataractDavid D Geyer, M Anne Spence, Meriam Johannes, et al.
The Journal of Biological Chemistry|June 15, 2007
Multiple and additive functions of ALDH3A1 and ALDH1A1: cataract phenotype and ocular oxidative damage in Aldh3a1(-/-)/Aldh1a1(-/-) knock-out miceNatalie Lassen, J Bronwyn Bateman, Tia Estey, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Ophthalmology|January 20, 2007
Gene conversion mutation in crystallin, beta-B2 (CRYBB2) in a Chilean family with autosomal dominant cataractJ Bronwyn Bateman, Fernando R Barria von-Bischhoffshaunsen, Leslie Richter, et al.
JAMA Ophthalmology|June 15, 2013
Distinct ocular expression in infants and children with Down syndrome in Cairo, Egypt: myopia and heart diseaseHanan H Afifi, Amira A Abdel Azeem, Hala T El-Bassyouni, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 13, 2002
Infantile cataract in the collaborative perinatal project: prevalence and risk factorsJohn Paul SanGiovanni, Emily Y Chew, George F Reed, et al.
American Journal of Medical Genetics. Part A|February 28, 2008
Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA)Leslie Richter, Pamela Flodman, Fernando Barria von-Bischhoffshausen, et al.
Investigative Ophthalmology & Visual Science|August 1, 2006
A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genesJ Bronwyn Bateman, Leslie Richter, Pamela Flodman, et al.
American Journal of Ophthalmology|March 28, 2006
Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataractDavid D Geyer, M Anne Spence, Meriam Johannes, et al.
The Journal of Biological Chemistry|June 15, 2007
Multiple and additive functions of ALDH3A1 and ALDH1A1: cataract phenotype and ocular oxidative damage in Aldh3a1(-/-)/Aldh1a1(-/-) knock-out miceNatalie Lassen, J Bronwyn Bateman, Tia Estey, et al.
Pageof 2