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R G Weleber

Showing results (41-50 of 110) with videos related to

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Retina (Philadelphia, Pa.)|January 1, 1997
Gyrate atrophy-like phenotype with normal plasma ornithineU Kellner, R G Weleber, N G Kennaway, et al.
Journal of Medical Genetics|November 19, 2008
Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual lossP J Francis, S C Hamon, J Ott, et al.
American Journal of Ophthalmology|August 15, 1990
Diagnostic clinical findings of a new syndrome with night blindness, maculopathy, and enhanced S cone sensitivityM F Marmor, S G Jacobson, M H Foerster, et al.
Investigative Ophthalmology & Visual Science|February 1, 1990
A histopathologic study of a choroideremia carrierJ G Flannery, A C Bird, D B Farber, et al.
Investigative Ophthalmology & Visual Science|December 31, 1997
Sperm abnormalities in retinitis pigmentosaW E Connor, R G Weleber, C DeFrancesco, et al.
The Journal of Pediatrics|January 1, 1986
Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four childrenS S Budden, N G Kennaway, N R Buist, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1996
Sorsby fundus dystrophy. A family with the Ser181Cys mutation of the tissue inhibitor of metalloproteinases 3R D Carrero-Valenzuela, M L Klein, R G Weleber, et al.
The British Journal of Ophthalmology|March 29, 2008
Acute zonal occult outer retinopathy (AZOOR) and pars planitis: a new association?S M Sharma, R C Watzke, R G Weleber, et al.
Human Molecular Genetics|April 18, 1998
Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAAM Litt, P Kramer, D M LaMorticella, 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.
Pageof 11

Showing results (41-50 of 110) with videos related to

Sort By:
Pageof 11
Retina (Philadelphia, Pa.)|January 1, 1997
Gyrate atrophy-like phenotype with normal plasma ornithineU Kellner, R G Weleber, N G Kennaway, et al.
Journal of Medical Genetics|November 19, 2008
Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual lossP J Francis, S C Hamon, J Ott, et al.
American Journal of Ophthalmology|August 15, 1990
Diagnostic clinical findings of a new syndrome with night blindness, maculopathy, and enhanced S cone sensitivityM F Marmor, S G Jacobson, M H Foerster, et al.
Investigative Ophthalmology & Visual Science|February 1, 1990
A histopathologic study of a choroideremia carrierJ G Flannery, A C Bird, D B Farber, et al.
Investigative Ophthalmology & Visual Science|December 31, 1997
Sperm abnormalities in retinitis pigmentosaW E Connor, R G Weleber, C DeFrancesco, et al.
The Journal of Pediatrics|January 1, 1986
Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four childrenS S Budden, N G Kennaway, N R Buist, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1996
Sorsby fundus dystrophy. A family with the Ser181Cys mutation of the tissue inhibitor of metalloproteinases 3R D Carrero-Valenzuela, M L Klein, R G Weleber, et al.
The British Journal of Ophthalmology|March 29, 2008
Acute zonal occult outer retinopathy (AZOOR) and pars planitis: a new association?S M Sharma, R C Watzke, R G Weleber, et al.
Human Molecular Genetics|April 18, 1998
Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAAM Litt, P Kramer, D M LaMorticella, 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.
Pageof 11