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Y Floderus

Showing results (1-10 of 34) with videos related to

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Clinical Genetics|May 1, 1981
The inheritance of human erythrocyte catechol-O-methyltransferase activityY Floderus, L Wetterberg
Clinical Genetics|May 1, 1981
Erythrocyte catechol-O-methyltransferase activity in psychotic twinsY Floderus, G Eberhard, L Witterberg
Clinical Genetics|July 16, 2003
Nine novel mutations in the protoporphyrinogen oxidase gene in Swedish families with variegate porphyriaA Wiman, P Harper, Y Floderus
Clinical Genetics|May 1, 1981
Erythrocyte catechol-O-methyltransferase activity in related families with schizophreniaY Floderus, J A Böök, L Wetterberg
Clinical Genetics|May 1, 1981
Erythrocyte catechol-O-methyltransferase activity in a Swedish populationY Floderus, S B Ross, L Wetterberg
Biochemical Genetics|October 1, 1975
Molecular nature of beta-galactosidase from different tissues in two strains of the house mouseR Seyedyazdani, Y Floderus, L G Lundin
Journal of Internal Medicine|April 24, 2010
Erythropoietic protoporphyria in Sweden: demographic, clinical, biochemical and genetic characteristicsS Wahlin, Y Floderus, P Stål, et al.
Human Heredity|January 1, 1982
Evidence for a major locus as well as a multifactorial component in the regulation of human red blood cell catechol-O-methyl-transferase activityY Floderus, L Iselius, J Lindsten, et al.
Clinical Genetics|October 10, 2002
Acute intermittent porphyria in Sweden. Molecular, functional and clinical consequences of some new mutations found in the porphobilinogen deaminase geneY Floderus, P M Shoolingin-Jordan, P Harper
Physiological Research|February 15, 2007
Porphyria in SwedenS Thunell, Y Floderus, A Henrichson, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Clinical Genetics|May 1, 1981
The inheritance of human erythrocyte catechol-O-methyltransferase activityY Floderus, L Wetterberg
Clinical Genetics|May 1, 1981
Erythrocyte catechol-O-methyltransferase activity in psychotic twinsY Floderus, G Eberhard, L Witterberg
Clinical Genetics|July 16, 2003
Nine novel mutations in the protoporphyrinogen oxidase gene in Swedish families with variegate porphyriaA Wiman, P Harper, Y Floderus
Clinical Genetics|May 1, 1981
Erythrocyte catechol-O-methyltransferase activity in related families with schizophreniaY Floderus, J A Böök, L Wetterberg
Clinical Genetics|May 1, 1981
Erythrocyte catechol-O-methyltransferase activity in a Swedish populationY Floderus, S B Ross, L Wetterberg
Biochemical Genetics|October 1, 1975
Molecular nature of beta-galactosidase from different tissues in two strains of the house mouseR Seyedyazdani, Y Floderus, L G Lundin
Journal of Internal Medicine|April 24, 2010
Erythropoietic protoporphyria in Sweden: demographic, clinical, biochemical and genetic characteristicsS Wahlin, Y Floderus, P Stål, et al.
Human Heredity|January 1, 1982
Evidence for a major locus as well as a multifactorial component in the regulation of human red blood cell catechol-O-methyl-transferase activityY Floderus, L Iselius, J Lindsten, et al.
Clinical Genetics|October 10, 2002
Acute intermittent porphyria in Sweden. Molecular, functional and clinical consequences of some new mutations found in the porphobilinogen deaminase geneY Floderus, P M Shoolingin-Jordan, P Harper
Physiological Research|February 15, 2007
Porphyria in SwedenS Thunell, Y Floderus, A Henrichson, et al.
Pageof 4