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J H Fingert

Showing results (1-10 of 20) with videos related to

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Eye (London, England)|May 13, 2011
Primary open-angle glaucoma genesJ H Fingert
Ophthalmic Genetics|December 28, 1999
Normal range of hearing associated with myocilin Thr377MetR M Simm, J H Fingert, J E Craig, et al.
Eye (London, England)|April 8, 2017
Assessment of a three-generation pedigree with Fuchs endothelial corneal dystrophy with anticipation for expansion of the triplet repeat in the TCF4 geneM A Greiner, D C Terveen, J M Vislisel, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1997
Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)J Brown, J H Fingert, C M Taylor, et al.
Investigative Ophthalmology & Visual Science|December 1, 2001
Delayed secondary glucocorticoid responsiveness of MYOC in human trabecular meshwork cellsA R Shepard, N Jacobson, J H Fingert, et al.
Eye (London, England)|January 20, 2018
A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigreeM J Schnieders, W Goar, M Griess, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 22, 1999
Clinical characterization and linkage analysis of a family with congenital X-linked nystagmus and deuteranomalyM L Mellott, J Brown, J H Fingert, 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.
Journal of Medical Genetics|December 1, 1998
A novel Asp380Ala mutation in the GLC1A/myocilin gene in a family with juvenile onset primary open angle glaucomaA M Kennan, F C Mansergh, J H Fingert, et al.
Genome Research|June 13, 1998
Characterization and comparison of the human and mouse GLC1A glaucoma genesJ H Fingert, L Ying, R E Swiderski, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Eye (London, England)|May 13, 2011
Primary open-angle glaucoma genesJ H Fingert
Ophthalmic Genetics|December 28, 1999
Normal range of hearing associated with myocilin Thr377MetR M Simm, J H Fingert, J E Craig, et al.
Eye (London, England)|April 8, 2017
Assessment of a three-generation pedigree with Fuchs endothelial corneal dystrophy with anticipation for expansion of the triplet repeat in the TCF4 geneM A Greiner, D C Terveen, J M Vislisel, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1997
Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)J Brown, J H Fingert, C M Taylor, et al.
Investigative Ophthalmology & Visual Science|December 1, 2001
Delayed secondary glucocorticoid responsiveness of MYOC in human trabecular meshwork cellsA R Shepard, N Jacobson, J H Fingert, et al.
Eye (London, England)|January 20, 2018
A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigreeM J Schnieders, W Goar, M Griess, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 22, 1999
Clinical characterization and linkage analysis of a family with congenital X-linked nystagmus and deuteranomalyM L Mellott, J Brown, J H Fingert, 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.
Journal of Medical Genetics|December 1, 1998
A novel Asp380Ala mutation in the GLC1A/myocilin gene in a family with juvenile onset primary open angle glaucomaA M Kennan, F C Mansergh, J H Fingert, et al.
Genome Research|June 13, 1998
Characterization and comparison of the human and mouse GLC1A glaucoma genesJ H Fingert, L Ying, R E Swiderski, et al.
Pageof 2