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R G Weleber

Showing results (81-90 of 93) with videos related to

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Investigative Ophthalmology & Visual Science|May 8, 2000
Allelic variation in the VMD2 gene in best disease and age-related macular degenerationA J Lotery, F L Munier, G A Fishman, et al.
Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Molecular Genetics and Metabolism|March 9, 1999
Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutantsD A Pillers, R G Weleber, D G Green, et al.
Human Mutation|May 12, 2009
Predicting the pathogenicity of RPE65 mutationsA R Philp, M Jin, S Li, et al.
Human Mutation|October 26, 1999
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence changeK T Hiriyanna, E L Bingham, B M Yashar, et al.
Human Genetics|September 10, 1999
Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutationsD A Pillers, K M Fitzgerald, N M Duncan, et al.
Investigative Ophthalmology & Visual Science|June 14, 2000
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosaS G Jacobson, A V Cideciyan, A Iannaccone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001
Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
An analysis of allelic variation in the ABCA4 geneA R Webster, E Héon, A J Lotery, et al.
Nature Genetics|November 4, 2000
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
Investigative Ophthalmology & Visual Science|May 8, 2000
Allelic variation in the VMD2 gene in best disease and age-related macular degenerationA J Lotery, F L Munier, G A Fishman, et al.
Investigative Ophthalmology & Visual Science|July 7, 1999
Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerationsY Q Gao, M Danciger, R Longmuir, et al.
Molecular Genetics and Metabolism|March 9, 1999
Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutantsD A Pillers, R G Weleber, D G Green, et al.
Human Mutation|May 12, 2009
Predicting the pathogenicity of RPE65 mutationsA R Philp, M Jin, S Li, et al.
Human Mutation|October 26, 1999
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence changeK T Hiriyanna, E L Bingham, B M Yashar, et al.
Human Genetics|September 10, 1999
Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutationsD A Pillers, K M Fitzgerald, N M Duncan, et al.
Investigative Ophthalmology & Visual Science|June 14, 2000
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosaS G Jacobson, A V Cideciyan, A Iannaccone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001
Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
An analysis of allelic variation in the ABCA4 geneA R Webster, E Héon, A J Lotery, et al.
Nature Genetics|November 4, 2000
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Pageof 10