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American Journal of Perinatology|September 1, 1995
Incidence, timing, and follow-up of periventricular leukomalaciaM C Goetz, R J Gretebeck, K S Oh, et al.
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.
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.
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.
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