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S Jagell

Showing results (21-30 of 29) with videos related to

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Hereditas|October 7, 1998
Detailed genetic and physical mapping in the Sjögren-Larsson syndrome gene region in 17p11.2A Sillén, A Alderborn, M Pigg, et al.
Acta Radiologica. Oncology|January 1, 1981
Microcephaly, mental retardation and chromosomal aberrations in a girl following radiation therapy during late fetal lifeK H Gustavson, S Jagell, H K Blomquist, et al.
Clinical Genetics|July 1, 1982
Catechol-o-methyltransferase activity in erythrocytes in Down's syndrome: family studiesK H Gustavson, Y Flodérus, S Jagell, et al.
Molecular and Chemical Neuropathology|August 1, 1991
Monoaminergic dysfunction in Sjögren-Larsson syndromeP Wester, U Bergström, A Brun, et al.
Journal of Child Neurology|August 2, 2000
D-2-hydroxyglutaric aciduria with cerebral, vascular, and muscular abnormalities in a 14-year-old boyO Eeg-Olofsson, W W Zhang, Y Olsson, et al.
Nature Genetics|December 1, 1994
The Sjögren-Larsson syndrome gene is close to D17S805 as determined by linkage analysis and allelic associationM Pigg, S Jagell, A Sillén, et al.
Acta Paediatrica Scandinavica|July 1, 1976
Low molecular weight proteinuria and slight hyperlipoproteinemia in three mentally retarded brothersR Eksmyr, G Fex, S Jagell, et al.
Human Mutation|November 26, 1998
Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndromeA Sillén, I Anton-Lamprecht, C Braun-Quentin, et al.
The Journal of Pediatrics|August 1, 1989
Sjögren-Larsson syndrome: inherited defect in the fatty alcohol cycleW B Rizzo, A L Dammann, D A Craft, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Hereditas|October 7, 1998
Detailed genetic and physical mapping in the Sjögren-Larsson syndrome gene region in 17p11.2A Sillén, A Alderborn, M Pigg, et al.
Acta Radiologica. Oncology|January 1, 1981
Microcephaly, mental retardation and chromosomal aberrations in a girl following radiation therapy during late fetal lifeK H Gustavson, S Jagell, H K Blomquist, et al.
Clinical Genetics|July 1, 1982
Catechol-o-methyltransferase activity in erythrocytes in Down's syndrome: family studiesK H Gustavson, Y Flodérus, S Jagell, et al.
Molecular and Chemical Neuropathology|August 1, 1991
Monoaminergic dysfunction in Sjögren-Larsson syndromeP Wester, U Bergström, A Brun, et al.
Journal of Child Neurology|August 2, 2000
D-2-hydroxyglutaric aciduria with cerebral, vascular, and muscular abnormalities in a 14-year-old boyO Eeg-Olofsson, W W Zhang, Y Olsson, et al.
Nature Genetics|December 1, 1994
The Sjögren-Larsson syndrome gene is close to D17S805 as determined by linkage analysis and allelic associationM Pigg, S Jagell, A Sillén, et al.
Acta Paediatrica Scandinavica|July 1, 1976
Low molecular weight proteinuria and slight hyperlipoproteinemia in three mentally retarded brothersR Eksmyr, G Fex, S Jagell, et al.
Human Mutation|November 26, 1998
Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndromeA Sillén, I Anton-Lamprecht, C Braun-Quentin, et al.
The Journal of Pediatrics|August 1, 1989
Sjögren-Larsson syndrome: inherited defect in the fatty alcohol cycleW B Rizzo, A L Dammann, D A Craft, et al.
Pageof 3