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Human Biology|October 1, 1991
Polymorphisms at VNTR loci suggest homogeneity of the white population of UtahR Chakraborty, S P DaigerAmerican 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.Biochemical Genetics|August 1, 1981
Human thyroxine-binding globulin (TBG): heterogeneity within individuals and among individuals demonstrated by isoelectric focusingS P Daiger, R S WildinMolecular Medicine Today|September 1, 1996
Inherited retinal degeneration: exceptional genetic and clinical heterogeneityL S Sullivan, S P DaigerNature 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.American Journal of Human Genetics|May 1, 1984
Heritability of quantitative variation at the group-specific component (Gc) locusS P Daiger, M Miller, R ChakrabortyAmerican Journal of Human Genetics|November 1, 1977
Detection of genetic variation with radioactive ligands. II. Genetic variants of vitamin D-labeled group-specific component (Gc) proteinsS P Daiger, L L Cavalli-SforzaAmerican Journal of Human Genetics|January 1, 1993
Evaluation of standard error and confidence interval of estimated multilocus genotype probabilities, and their implications in DNA forensicsR Chakraborty, M R Srinivasan, S P DaigerGenomics|May 1, 1997
Localization and characterization of the human ADP-ribosylation factor 5 (ARF5) geneR E McGuire, S P Daiger, E D GreenClinical Genetics|May 25, 2013
Genes and mutations causing retinitis pigmentosaS P Daiger, L S Sullivan, S J BownePageof 12