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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.
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.
Molecular Medicine Today|September 1, 1996
Inherited retinal degeneration: exceptional genetic and clinical heterogeneityL S Sullivan, S P Daiger
Chinese Medical Journal|June 1, 1992
Linkage between Rh blood group and autosomal dominant retinitis pigmentosa in ten Chinese familiesY J Fei, S H Blanton, S P Daiger, et al.
Clinical Genetics|May 25, 2013
Genes and mutations causing retinitis pigmentosaS P Daiger, L S Sullivan, S J Bowne
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|June 1, 1993
Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13AJ T Hecht, Y Wang, B Connor, et al.
Molecular Vision|May 6, 1999
Identifying and mapping novel retinal-expressed ESTs from humansK Malone, M M Sohocki, L S Sullivan, et al.
American Journal of Human Genetics|September 1, 1991
Cleft lip and palate: no evidence of linkage to transforming growth factor alphaJ T Hecht, Y P Wang, S H Blanton, 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.
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