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R Matalon

Showing results (31-40 of 185) with videos related to

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Lancet (London, England)|April 16, 1977
Phenylalanine hydroxylase in human placenta: novel system for study of phenylketonuriaR Matalon, P Justice, M N Deanching
New York State Journal of Medicine|April 1, 1984
Vascular access for patients on long-term hemodialysis maintenanceG E Kim, H Hovaguimian, R Matalon
Molecular Syndromology|March 12, 2015
Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial SynpolydactylyK Meyertholen, J B Ravnan, R Matalon
Lancet (London, England)|April 8, 1972
A chemical method for the antenatal diagnosis of mucopolysaccharidosesR Matalon, A Dorfman, H L Nadler
Biochemical and Biophysical Research Communications|January 22, 1971
L-iduronidase in cultured human fibroblasts and liverR Matalon, J A Cifonelli, A Dorfman
Birth Defects Original Article Series|March 1, 1973
Enzyme replacement in Fabry disease: treatment of cultured skin fibroblasts with a purified alpha-galactosidase from ficinG Dawson, R Matalon, Y T Li
The Journal of Pediatrics|September 1, 1971
Lactosylceramidosis: lactosylceramide galactosyl hydrolase deficiency and accumulation of lactosylceramide in cultured skin fibroblastsG Dawson, R Matalon, A O Stein
Analytical Chemistry|March 1, 1977
Automated cleanup of herbicides by adsorption chromatography for the determination of 2,3,7,8-tetrachlorodibenzo-p-dioxinT Ramstad, N H Mahle, R Matalon
American Journal of Medical Genetics|January 1, 1987
Dominant inheritance of a syndrome similar to Rubinstein-TaybiP Cotsirilos, J C Taylor, R Matalon
The Journal of Clinical Investigation|September 1, 1975
Glycopeptide storage in skin fibroblasts cultured from a patient with alpha-mannosidase deficiencyG C Tsay, G Dawson, R Matalon
Pageof 19

Showing results (31-40 of 185) with videos related to

Sort By:
Pageof 19
Lancet (London, England)|April 16, 1977
Phenylalanine hydroxylase in human placenta: novel system for study of phenylketonuriaR Matalon, P Justice, M N Deanching
New York State Journal of Medicine|April 1, 1984
Vascular access for patients on long-term hemodialysis maintenanceG E Kim, H Hovaguimian, R Matalon
Molecular Syndromology|March 12, 2015
Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial SynpolydactylyK Meyertholen, J B Ravnan, R Matalon
Lancet (London, England)|April 8, 1972
A chemical method for the antenatal diagnosis of mucopolysaccharidosesR Matalon, A Dorfman, H L Nadler
Biochemical and Biophysical Research Communications|January 22, 1971
L-iduronidase in cultured human fibroblasts and liverR Matalon, J A Cifonelli, A Dorfman
Birth Defects Original Article Series|March 1, 1973
Enzyme replacement in Fabry disease: treatment of cultured skin fibroblasts with a purified alpha-galactosidase from ficinG Dawson, R Matalon, Y T Li
The Journal of Pediatrics|September 1, 1971
Lactosylceramidosis: lactosylceramide galactosyl hydrolase deficiency and accumulation of lactosylceramide in cultured skin fibroblastsG Dawson, R Matalon, A O Stein
Analytical Chemistry|March 1, 1977
Automated cleanup of herbicides by adsorption chromatography for the determination of 2,3,7,8-tetrachlorodibenzo-p-dioxinT Ramstad, N H Mahle, R Matalon
American Journal of Medical Genetics|January 1, 1987
Dominant inheritance of a syndrome similar to Rubinstein-TaybiP Cotsirilos, J C Taylor, R Matalon
The Journal of Clinical Investigation|September 1, 1975
Glycopeptide storage in skin fibroblasts cultured from a patient with alpha-mannosidase deficiencyG C Tsay, G Dawson, R Matalon
Pageof 19