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R G Weleber

Showing results (31-40 of 110) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1978
Aicardi's syndrome. Case report, clinical features, and electrophysiologic studiesR G Weleber, E W Lovrien, J B Isom
Retina (Philadelphia, Pa.)|January 1, 1987
Non-Hodgkin's lymphoma causing fundus picture simulating fundus flavimaculatusJ D Gass, R G Weleber, D R Johnson
American Journal of Ophthalmology|October 15, 1986
Ophthalmologic and systemic manifestations of Alström's diseaseR H Millay, R G Weleber, J R Heckenlively
Human Genetics|November 1, 1992
A single-base change at a splice acceptor site in the ornithine aminotransferase gene causes abnormal RNA splicing in gyrate atrophyY Mashima, R G Weleber, N G Kennaway, et al.
American Journal of Human Genetics|March 1, 1989
Inheritance of ornithine aminotransferase gene, mRNA, and enzyme defect in a family with gyrate atrophy of the choroid and retinaY Hotta, N G Kennaway, R G Weleber, et al.
American Journal of Human Genetics|March 1, 1989
Gyrate atrophy of the choroid and retina: characterization of mutant ornithine aminotransferase and mechanism of response to vitamin B6N G Kennaway, L Stankova, M K Wirtz, et al.
Ophthalmic Genetics|January 5, 2000
Genotype-phenotype correlation of a pyridoxine-responsive form of gyrate atrophyY G Mashima, R G Weleber, N G Kennaway, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1986
Abnormal retinal function associated with isotretinoin therapy for acneR G Weleber, S T Denman, J M Hanifin, et al.
Annales De Genetique|December 1, 1972
Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome IIR E Magenis, S Armendares, F Hecht, et al.
Journal of Pediatric Ophthalmology and Strabismus|February 24, 2001
Ophthalmologic screening of deaf students in OregonM V Brinks, W H Murphey, W Cardwell, et al.
Pageof 11

Showing results (31-40 of 110) with videos related to

Sort By:
Pageof 11
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1978
Aicardi's syndrome. Case report, clinical features, and electrophysiologic studiesR G Weleber, E W Lovrien, J B Isom
Retina (Philadelphia, Pa.)|January 1, 1987
Non-Hodgkin's lymphoma causing fundus picture simulating fundus flavimaculatusJ D Gass, R G Weleber, D R Johnson
American Journal of Ophthalmology|October 15, 1986
Ophthalmologic and systemic manifestations of Alström's diseaseR H Millay, R G Weleber, J R Heckenlively
Human Genetics|November 1, 1992
A single-base change at a splice acceptor site in the ornithine aminotransferase gene causes abnormal RNA splicing in gyrate atrophyY Mashima, R G Weleber, N G Kennaway, et al.
American Journal of Human Genetics|March 1, 1989
Inheritance of ornithine aminotransferase gene, mRNA, and enzyme defect in a family with gyrate atrophy of the choroid and retinaY Hotta, N G Kennaway, R G Weleber, et al.
American Journal of Human Genetics|March 1, 1989
Gyrate atrophy of the choroid and retina: characterization of mutant ornithine aminotransferase and mechanism of response to vitamin B6N G Kennaway, L Stankova, M K Wirtz, et al.
Ophthalmic Genetics|January 5, 2000
Genotype-phenotype correlation of a pyridoxine-responsive form of gyrate atrophyY G Mashima, R G Weleber, N G Kennaway, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1986
Abnormal retinal function associated with isotretinoin therapy for acneR G Weleber, S T Denman, J M Hanifin, et al.
Annales De Genetique|December 1, 1972
Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome IIR E Magenis, S Armendares, F Hecht, et al.
Journal of Pediatric Ophthalmology and Strabismus|February 24, 2001
Ophthalmologic screening of deaf students in OregonM V Brinks, W H Murphey, W Cardwell, et al.
Pageof 11