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Clinical Genetics|February 1, 1975
A familial F/G translocation [t(p-; 22q+)] observed in three generationsM M Cohen, R G Davidson, J A BrownAmerican Journal of Human Genetics|March 1, 1976
Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosisM C Rattazzi, J A Brown, R G Davidson, et al.Pediatrics|June 1, 1988
Atlantoaxial instability in individuals with Down syndrome: a fresh look at the evidenceR G DavidsonAmerican Journal of Human Genetics|September 1, 1980
Gaucher disease. III. Substrate specificity of glucocerebrosidase and the use of nonlabeled natural substrates for the investigation of patientsF Y Choy, R G DavidsonProceedings of the National Academy of Sciences of the United States of America|October 1, 1980
Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblastsP L Chang, R G DavidsonProceedings of the National Academy of Sciences of the United States of America|December 1, 1983
Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophyP L Chang, R G DavidsonPediatric Research|October 1, 1977
Prenatal diagnosis of metachromatic leukodystrophy by electrophoretic and immunologic techniquesM C Rattazzi, R G DavidsonPediatric Research|January 1, 1980
Gaucher's disease II. Studies on the kinetics of beta-glucosidase and the effects of sodium taurocholate in normal and Gaucher tissuesF Y Choy, R G DavidsonAmerican Journal of Medical Genetics|August 1, 1987
Neonatal manifestations of Schwartz-Jampel syndromeS A Farrell, R G Davidson, P ThorpNeurobehavioral Toxicology and Teratology|January 1, 1981
Neoplasia and the fetal alcohol and hydantoin syndromesM M CohenPageof 76