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S P Daiger

Showing results (71-80 of 84) with videos related to

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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.
American Journal of Human Genetics|April 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locusD G Bradley, G J Farrar, E M Sharp, et al.
American Journal of Human Genetics|October 11, 1992
Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhereH Northrup, D J Kwiatkowski, E S Roach, et al.
Genomics|September 1, 1992
Human chromosome 8 linkage map based on short tandem repeat polymorphisms: effect of genotyping errorsJ Tomfohrde, S Wood, M Schertzer, et al.
Genomics|December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11R J Smith, E C Lee, W J Kimberling, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Report and abstracts of the First International Workshop on Human Chromosome 8 Mapping. Vancouver, British Columbia, May 2-4, 1993S Wood, K Ben Othmane, U S Bergerheim, et al.
American Journal of Medical Genetics|June 1, 1994
Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysisL Ni, M J Wagner, W J Kimberling, et al.
American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, 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.
Molecular Genetics and Metabolism|June 30, 2000
Prevalence of AIPL1 mutations in inherited retinal degenerative diseaseM M Sohocki, I Perrault, B P Leroy, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
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.
American Journal of Human Genetics|April 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locusD G Bradley, G J Farrar, E M Sharp, et al.
American Journal of Human Genetics|October 11, 1992
Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhereH Northrup, D J Kwiatkowski, E S Roach, et al.
Genomics|September 1, 1992
Human chromosome 8 linkage map based on short tandem repeat polymorphisms: effect of genotyping errorsJ Tomfohrde, S Wood, M Schertzer, et al.
Genomics|December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11R J Smith, E C Lee, W J Kimberling, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Report and abstracts of the First International Workshop on Human Chromosome 8 Mapping. Vancouver, British Columbia, May 2-4, 1993S Wood, K Ben Othmane, U S Bergerheim, et al.
American Journal of Medical Genetics|June 1, 1994
Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysisL Ni, M J Wagner, W J Kimberling, et al.
American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, 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.
Molecular Genetics and Metabolism|June 30, 2000
Prevalence of AIPL1 mutations in inherited retinal degenerative diseaseM M Sohocki, I Perrault, B P Leroy, et al.
Pageof 9