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P F Benson

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Clinical Genetics|November 1, 1979
Prenatal diagnosis of galactosaemia in six pregnancies -- possible complications with rare alleles of the galactose 1-phosphate uridyl transferase locusP F Benson, N J Brandt, E Christensen, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Fibroblast alpha-galactosidase A activity for identification of Fabry's disease heterozygotesA H Fensom, P F Benson, A R Grant, et al.
American Journal of Human Genetics|September 1, 1980
Prenatal diagnosis of argininosuccinic aciduria: effect of mycoplasma contamination on the indirect assay for argininosuccinate lyaseA H Fensom, P F Benson, J E Baker, et al.
Clinical Genetics|November 1, 1979
Lumbar kyphosis in Hunter's disease (MPS ii)P F Benson, L R Button, A H Fensom, et al.
The Journal of Hygiene|March 1, 1972
Detection of Bordetella pertussis antibodies in human sera by complement-fixation and immunofluorescenceC M Bradstreet, A J Tannahill, J M Edwards, et al.
Archives of Disease in Childhood|February 1, 1972
Substrate induction of galactokinase in cultured fibroblasts from subjects heterozygous and homozygous for galactokinase deficiencyF Zacchello, P F Benson, P Croll, et al.
Lancet (London, England)|August 25, 1979
Gestational age at termination of pregnancy on medical indicationsP E Polani, P F Benson, S Blunt, et al.
Guy'S Hospital Reports|January 1, 1972
Pompe's disease--detection of maternal heterozygote and antenatal exclusion in the fetusP F Benson, S Blunt, S P Brown, et al.
Journal of Medical Genetics|April 1, 1976
Amniotic cell 4-methylumbelliferyl-alpha-glucosidase activity for prenatal diagnosis of Pompe's diseaseA H Fensom, P F Benson, S Blunt, et al.
Lancet (London, England)|January 21, 1978
Fluorimetric assay for prenatal detection of Hurler and Scheie homozygotes or heterozygotesJ L Stirling, D Robinson, A H Fensom, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
Clinical Genetics|November 1, 1979
Prenatal diagnosis of galactosaemia in six pregnancies -- possible complications with rare alleles of the galactose 1-phosphate uridyl transferase locusP F Benson, N J Brandt, E Christensen, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Fibroblast alpha-galactosidase A activity for identification of Fabry's disease heterozygotesA H Fensom, P F Benson, A R Grant, et al.
American Journal of Human Genetics|September 1, 1980
Prenatal diagnosis of argininosuccinic aciduria: effect of mycoplasma contamination on the indirect assay for argininosuccinate lyaseA H Fensom, P F Benson, J E Baker, et al.
Clinical Genetics|November 1, 1979
Lumbar kyphosis in Hunter's disease (MPS ii)P F Benson, L R Button, A H Fensom, et al.
The Journal of Hygiene|March 1, 1972
Detection of Bordetella pertussis antibodies in human sera by complement-fixation and immunofluorescenceC M Bradstreet, A J Tannahill, J M Edwards, et al.
Archives of Disease in Childhood|February 1, 1972
Substrate induction of galactokinase in cultured fibroblasts from subjects heterozygous and homozygous for galactokinase deficiencyF Zacchello, P F Benson, P Croll, et al.
Lancet (London, England)|August 25, 1979
Gestational age at termination of pregnancy on medical indicationsP E Polani, P F Benson, S Blunt, et al.
Guy'S Hospital Reports|January 1, 1972
Pompe's disease--detection of maternal heterozygote and antenatal exclusion in the fetusP F Benson, S Blunt, S P Brown, et al.
Journal of Medical Genetics|April 1, 1976
Amniotic cell 4-methylumbelliferyl-alpha-glucosidase activity for prenatal diagnosis of Pompe's diseaseA H Fensom, P F Benson, S Blunt, et al.
Lancet (London, England)|January 21, 1978
Fluorimetric assay for prenatal detection of Hurler and Scheie homozygotes or heterozygotesJ L Stirling, D Robinson, A H Fensom, et al.
Pageof 8