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The Journal of Heredity|March 1, 1991
Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouseH O Sweet, R T BronsonThe Journal of Heredity|March 1, 1996
Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouseH O Sweet, R T Bronson, L R Donahue, et al.Journal of Neurogenetics|May 1, 1992
Genetic and age related models of neurodegeneration in mice: dystrophic axonsR T Bronson, H O Sweet, C A Spencer, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 1, 1996
Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migrationH O Sweet, R T Bronson, K R Johnson, et al.Human Molecular Genetics|June 13, 1998
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactylyK R Johnson, H O Sweet, L R Donahue, et al.The Journal of Endocrinology|April 1, 1994
Adrenocortical dysplasia: a mouse model system for adrenocortical insufficiencyW G Beamer, H O Sweet, R T Bronson, et al.The Journal of Heredity|July 1, 1983
Dilute suppressor, a new suppressor gene in the house mouseH O SweetBrain, Behavior and Evolution|January 1, 1979
Brain weight-body weight scaling in breeds of dogs and catsR T BronsonAmerican Journal of Veterinary Research|November 1, 1982
Variation in age at death of dogs of different sexes and breedsR T BronsonJournal of the Neurological Sciences|July 1, 1980
Necrotizing myopathy associated with hemolytic anemia in owl monkeys (Aotus trivirgatus)R T BronsonPageof 20