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L S Sullivan

Showing results (1-10 of 18) with videos related to

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American Journal of Diseases of Children (1960)|April 1, 1985
Feeding intolerance following ophthalmologic examinationM C Hermansen, L S Sullivan
Molecular Medicine Today|September 1, 1996
Inherited retinal degeneration: exceptional genetic and clinical heterogeneityL S Sullivan, S P Daiger
Clinical Genetics|May 25, 2013
Genes and mutations causing retinitis pigmentosaS P Daiger, L S Sullivan, S J Bowne
Molecular Vision|May 6, 1999
Identifying and mapping novel retinal-expressed ESTs from humansK Malone, M M Sohocki, L S Sullivan, et al.
Genomics|May 20, 1999
Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disordersM M Sohocki, K A Malone, L S Sullivan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 23, 2001
Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humansM M Sohocki, L S Sullivan, D L Tirpak, et al.
Human Genetics|January 1, 1995
Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated familyR E McGuire, A M Gannon, L S Sullivan, et al.
Human Molecular Genetics|February 1, 1994
Tetranucleotide repeat polymorphism (D8S582) for human EST00680 (D8S340E)L S Sullivan, J Parrish, M J Wagner, et al.
American Journal of Human Genetics|July 1, 1995
X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11R E McGuire, L S Sullivan, S H Blanton, et al.
American Journal of Human Genetics|July 1, 1997
Exclusion of atypical vitelliform macular dystrophy from 8q24.3 and from other known macular degenerative lociM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
American Journal of Diseases of Children (1960)|April 1, 1985
Feeding intolerance following ophthalmologic examinationM C Hermansen, L S Sullivan
Molecular Medicine Today|September 1, 1996
Inherited retinal degeneration: exceptional genetic and clinical heterogeneityL S Sullivan, S P Daiger
Clinical Genetics|May 25, 2013
Genes and mutations causing retinitis pigmentosaS P Daiger, L S Sullivan, S J Bowne
Molecular Vision|May 6, 1999
Identifying and mapping novel retinal-expressed ESTs from humansK Malone, M M Sohocki, L S Sullivan, et al.
Genomics|May 20, 1999
Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disordersM M Sohocki, K A Malone, L S Sullivan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 23, 2001
Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humansM M Sohocki, L S Sullivan, D L Tirpak, et al.
Human Genetics|January 1, 1995
Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated familyR E McGuire, A M Gannon, L S Sullivan, et al.
Human Molecular Genetics|February 1, 1994
Tetranucleotide repeat polymorphism (D8S582) for human EST00680 (D8S340E)L S Sullivan, J Parrish, M J Wagner, et al.
American Journal of Human Genetics|July 1, 1995
X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11R E McGuire, L S Sullivan, S H Blanton, et al.
American Journal of Human Genetics|July 1, 1997
Exclusion of atypical vitelliform macular dystrophy from 8q24.3 and from other known macular degenerative lociM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.
Pageof 2