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Nucleic Acids Research|January 25, 1990
Characterization of the promoter region of Tetrahymena genesC F Brunk, L A SadlerAmerican Journal of Human Genetics|June 1, 1988
Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLAH Y Zoghbi, S P Daiger, A McCall, et al.Journal of Medical Genetics|November 1, 1995
Evaluation of candidate genes for familial brachydactylyJ M Mastrobattista, P Dollé, S H Blanton, et al.American Journal of Human Genetics|March 1, 1978
Detection of genetic variation with radioactive ligands. III. genetic polymorphism of transcobalamin II in human plasmaS P Daiger, M L Labowe, M Parsons, et al.Lancet (London, England)|February 1, 1986
Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus in prenatal diagnosis of phenylketonuriaS P Daiger, A S Lidsky, R Chakraborty, 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 Medical Genetics|August 1, 1994
XLPRA: a canine retinal degeneration inherited as an X-linked traitG M Acland, S H Blanton, B Hershfield, et al.Genomics|January 1, 1993
Linkage studies of the esterase D and retinoblastoma genes to canine copper toxicosis: a model for Wilson diseaseV Yuzbasiyan-Gurkan, S Wagnitz, S H Blanton, et al.American Journal of Medical Genetics|August 1, 1992
Clinical variability and genetic heterogeneity within the Acadian Usher populationR J Smith, M Z Pelias, S P Daiger, et al.Pageof 12