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Y Ben-Yoseph

Showing results (11-20 of 44) with videos related to

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American Journal of Human Genetics|November 1, 1978
The nature of mutation in Krabbe diseaseY Ben-Yoseph, M Hungerford, H L Nadler
Clinical Genetics|January 1, 1988
First trimester prenatal evaluation for I-cell disease by N-acetyl-glucosamine 1-phosphotransferase assayY Ben-Yoseph, D A Mitchell, H L Nadler
Biochimica Et Biophysica Acta|October 8, 1982
Mannosylation of glycoproteins and dolichol derivatives in fibroblasts from patients with cystic fibrosisY Ben-Yoseph, C L DeFranco, H L Nadler
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1979
Decreased sialic acid and altered binding to lectins of purified alpha 2-macroglobulin from patients with cystic fibrosisY Ben-Yoseph, C L Defranco, H L Nadler
Pediatric Research|May 1, 1981
The metabolism of sialic acid in cystic fibrosisY Ben-Yoseph, C L Defranco, H L Nadler
The American Journal of the Medical Sciences|June 1, 1989
Prenatal diagnosis of I-cell disease in the first and second trimestersM R Parvathy, D A Mitchell, Y Ben-Yoseph
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1978
Lactosyl ceramidosis: deficient activity of neutral beta-galactosidase in liver and cultivated fibroblasts?B K Burton, Y Ben-Yoseph, H L Nadler
American Journal of Human Genetics|November 1, 1977
Quantitation of the enzymically deficient cross reacting material in GM1 gangliosidosesY Ben-Yoseph, B K Burton, H L Nadler
Human Mutation|April 17, 1999
A novel mutation (V191G) in a German-British type 1 Gaucher disease patient. Mutations in brief no. 131. OnlineF Y Choy, M L Humphries, Y Ben-Yoseph
The Biochemical Journal|January 1, 1979
Binding of human liver hydrolases by immobilized lectinsM B Fiddler, Y Ben-Yoseph, H L Nadler
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|November 1, 1978
The nature of mutation in Krabbe diseaseY Ben-Yoseph, M Hungerford, H L Nadler
Clinical Genetics|January 1, 1988
First trimester prenatal evaluation for I-cell disease by N-acetyl-glucosamine 1-phosphotransferase assayY Ben-Yoseph, D A Mitchell, H L Nadler
Biochimica Et Biophysica Acta|October 8, 1982
Mannosylation of glycoproteins and dolichol derivatives in fibroblasts from patients with cystic fibrosisY Ben-Yoseph, C L DeFranco, H L Nadler
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1979
Decreased sialic acid and altered binding to lectins of purified alpha 2-macroglobulin from patients with cystic fibrosisY Ben-Yoseph, C L Defranco, H L Nadler
Pediatric Research|May 1, 1981
The metabolism of sialic acid in cystic fibrosisY Ben-Yoseph, C L Defranco, H L Nadler
The American Journal of the Medical Sciences|June 1, 1989
Prenatal diagnosis of I-cell disease in the first and second trimestersM R Parvathy, D A Mitchell, Y Ben-Yoseph
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1978
Lactosyl ceramidosis: deficient activity of neutral beta-galactosidase in liver and cultivated fibroblasts?B K Burton, Y Ben-Yoseph, H L Nadler
American Journal of Human Genetics|November 1, 1977
Quantitation of the enzymically deficient cross reacting material in GM1 gangliosidosesY Ben-Yoseph, B K Burton, H L Nadler
Human Mutation|April 17, 1999
A novel mutation (V191G) in a German-British type 1 Gaucher disease patient. Mutations in brief no. 131. OnlineF Y Choy, M L Humphries, Y Ben-Yoseph
The Biochemical Journal|January 1, 1979
Binding of human liver hydrolases by immobilized lectinsM B Fiddler, Y Ben-Yoseph, H L Nadler
Pageof 5