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O Jensson

Showing results (21-30 of 102) with videos related to

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Nucleic Acids Research|December 25, 1990
Three RFLPs at the 3' end of the cystatin C gene, the disease gene in hereditary cystatin C amyloid angiopathy (HCCAA) in IcelandA Palsdottir, S Jonsdottir, M Abrahamson, et al.
Nordisk Medicin|January 1, 1994
[Transfusion medicine--Scandinavian recommendations]J Jørgensen, O Jensson, J Eklund, et al.
Nordisk Medicin|January 1, 1991
[Scandinavian recommendations for transfusion medicine]J Eklund, J Jørgensen, C Högman, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|February 1, 1990
The amino terminal portion of cerebrospinal fluid cystatin C in hereditary cystatin C amyloid angiopathy is not truncated: direct sequence analysis from agarose gel electropherogramsI Olafsson, G Gudmundsson, M Abrahamson, et al.
Human Heredity|January 1, 1983
Gc subtypes in Northern IndiansS Karlsson, I Skaftadóttir, A Arnason, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|January 1, 1997
Microvascular degeneration in hereditary cystatin C amyloid angiopathy of the brainZ Z Wang, O Jensson, L Thorsteinsson, et al.
Journal of Medical Genetics|December 1, 1972
Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individualsH Hauksdóttir, S Halldórsson, O Jensson, et al.
Nordisk Medicin|January 1, 1989
[Norwegian propositions for blood transfusion practices]C Högman, O Jensson, J Eklund, et al.
Nordisk Medicin|January 1, 1990
[Recommendations from the 12th Scandinavian meeting on transfusion medicine]J Eklund, J Jørgensen, C Högman, et al.
Acta Medica Scandinavica|January 1, 1982
Selective serum IgA deficiency in Icelanders. Frequency, family studies and Ig levelsJ Ulfarsson, S Gudmundsson, B Birgisdóttir, et al.
Pageof 11

Showing results (21-30 of 102) with videos related to

Sort By:
Pageof 11
Nucleic Acids Research|December 25, 1990
Three RFLPs at the 3' end of the cystatin C gene, the disease gene in hereditary cystatin C amyloid angiopathy (HCCAA) in IcelandA Palsdottir, S Jonsdottir, M Abrahamson, et al.
Nordisk Medicin|January 1, 1994
[Transfusion medicine--Scandinavian recommendations]J Jørgensen, O Jensson, J Eklund, et al.
Nordisk Medicin|January 1, 1991
[Scandinavian recommendations for transfusion medicine]J Eklund, J Jørgensen, C Högman, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|February 1, 1990
The amino terminal portion of cerebrospinal fluid cystatin C in hereditary cystatin C amyloid angiopathy is not truncated: direct sequence analysis from agarose gel electropherogramsI Olafsson, G Gudmundsson, M Abrahamson, et al.
Human Heredity|January 1, 1983
Gc subtypes in Northern IndiansS Karlsson, I Skaftadóttir, A Arnason, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|January 1, 1997
Microvascular degeneration in hereditary cystatin C amyloid angiopathy of the brainZ Z Wang, O Jensson, L Thorsteinsson, et al.
Journal of Medical Genetics|December 1, 1972
Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individualsH Hauksdóttir, S Halldórsson, O Jensson, et al.
Nordisk Medicin|January 1, 1989
[Norwegian propositions for blood transfusion practices]C Högman, O Jensson, J Eklund, et al.
Nordisk Medicin|January 1, 1990
[Recommendations from the 12th Scandinavian meeting on transfusion medicine]J Eklund, J Jørgensen, C Högman, et al.
Acta Medica Scandinavica|January 1, 1982
Selective serum IgA deficiency in Icelanders. Frequency, family studies and Ig levelsJ Ulfarsson, S Gudmundsson, B Birgisdóttir, et al.
Pageof 11