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L S Sullivan

Showing results (11-20 of 18) with videos related to

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Genomics|March 1, 1997
Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sitesM M Sohocki, L S Sullivan, W R Harrison, et al.
Molecular Vision|March 9, 2000
Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7qS J Bowne, L S Sullivan, L Ding, et al.
Genomics|December 24, 1997
Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24R W Yee, L S Sullivan, H T Lai, et al.
American Journal of Human Genetics|October 30, 1998
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor geneM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.
Nature Genetics|July 3, 1999
Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosaL S Sullivan, J R Heckenlively, S J Bowne, et al.
Human Mutation|January 4, 2001
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathiesM M Sohocki, S P Daiger, S J Bowne, et al.
Human Molecular Genetics|September 15, 1999
Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosaS J Bowne, S P Daiger, M M Hims, et al.
Nature Genetics|December 30, 1999
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosisM M Sohocki, S J Bowne, L S Sullivan, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Genomics|March 1, 1997
Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sitesM M Sohocki, L S Sullivan, W R Harrison, et al.
Molecular Vision|March 9, 2000
Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7qS J Bowne, L S Sullivan, L Ding, et al.
Genomics|December 24, 1997
Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24R W Yee, L S Sullivan, H T Lai, et al.
American Journal of Human Genetics|October 30, 1998
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor geneM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.
Nature Genetics|July 3, 1999
Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosaL S Sullivan, J R Heckenlively, S J Bowne, et al.
Human Mutation|January 4, 2001
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathiesM M Sohocki, S P Daiger, S J Bowne, et al.
Human Molecular Genetics|September 15, 1999
Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosaS J Bowne, S P Daiger, M M Hims, et al.
Nature Genetics|December 30, 1999
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosisM M Sohocki, S J Bowne, L S Sullivan, et al.
Pageof 2