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Clinical Chemistry|July 1, 1978
Hexosaminidase A in amniotic fluid of Tay-Sachs fetusesB Geiger, R Navon, R Arnon
Biochemical and Biophysical Research Communications|February 29, 1984
Hexosaminidase A deficient adults: presence of alpha chain precursor in cultured skin fibroblastsA Frisch, D Baram, R Navon
American Journal of Human Genetics|August 1, 1992
Identification and rapid detection of three Tay-Sachs mutations in the Moroccan Jewish populationL Drucker, R L Proia, R Navon
Human Mutation|January 1, 1997
Two mutated HEXA alleles in a Druze patient with late-infantile Tay-Sachs diseaseL Drucker, J A Hemli, R Navon
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1978
Phosphate metabolites in lymphoid, Friend erythroleukemia, and HeLa cells observed by high-resolution 31P nuclear magnetic resonanceG Navon, R Navon, R G Shulman, et al.
European Journal of Biochemistry|August 1, 1975
Specific determination of N-acetyl-beta-D-hexosaminidase isozymes A and B by radioimmunoassay and radial immunodiffusionB Geiger, R Navon, Y Ben-Yoseph, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 14, 1983
Tay-Sachs disease: one-step assay of beta-N-acetylhexosaminidase in serum with a sulphated chromogenic substrateW Fuchs, R Navon, M M Kaback, et al.
American Journal of Human Genetics|July 1, 1976
Low levels of beta hexosaminidase A in healthy individuals with apparent deficiency of this enzymeR Navon, B Geiger, Y B Yoseph, et al.
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