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O Jensson

Showing results (31-40 of 102) with videos related to

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British Medical Journal|November 11, 1972
Familial acute myeloid leukaemia with acquired Pelger-Huet anomaly and aneuploidy of C groupJ Kaur, D Catovsky, H Valdimarsson, et al.
Immunogenetics|January 1, 1987
Heterogeneity of human C4 gene size. A large intron (6.5 kb) is present in all C4A genes and some C4B genesA Palsdottir, R Fossdal, A Arnason, et al.
Human Mutation|January 1, 1992
Missense mutations causing mild hemophilia A in Iceland detected by denaturing gradient gel electrophoresisS Jonsdottir, C Diamond, B Levinson, et al.
American Journal of Human Genetics|May 1, 1995
Wilson disease in Iceland: a clinical and genetic studyG R Thomas, O Jensson, G Gudmundsson, et al.
The New England Journal of Medicine|December 13, 1984
Abnormal metabolism of gamma-trace alkaline microprotein. The basic defect in hereditary cerebral hemorrhage with amyloidosisA Grubb, O Jensson, G Gudmundsson, et al.
Journal of Medical Genetics|April 1, 1988
A family showing apparent X linked inheritance of both anencephaly and spina bifidaO Jensson, A Arnason, H Gunnarsdottir, et al.
Acta Medica Scandinavica|January 1, 1982
Serum amyloid P-component and C-reactive protein in serum of healthy Icelanders and members of an Icelandic family with macroglobulinaemiaO Jensson, O G Björnsson, A Arnason, et al.
Acta Medica Scandinavica|January 1, 1978
Macroglobulinaemia in an Icelandic familyO G Björnsson, A Arnason, S Gudmunosson, et al.
Scandinavian Journal of Immunology|September 1, 1990
The first Icelandic family with X-linked agammaglobulinaemia: studies of genetic markers and immune functionL Thorsteinsson, H M Ogmundsdóttir, A Sigfússon, et al.
Lancet (London, England)|September 10, 1988
Mutation in cystatin C gene causes hereditary brain haemorrhageA Palsdottir, M Abrahamson, L Thorsteinsson, et al.
Pageof 11

Showing results (31-40 of 102) with videos related to

Sort By:
Pageof 11
British Medical Journal|November 11, 1972
Familial acute myeloid leukaemia with acquired Pelger-Huet anomaly and aneuploidy of C groupJ Kaur, D Catovsky, H Valdimarsson, et al.
Immunogenetics|January 1, 1987
Heterogeneity of human C4 gene size. A large intron (6.5 kb) is present in all C4A genes and some C4B genesA Palsdottir, R Fossdal, A Arnason, et al.
Human Mutation|January 1, 1992
Missense mutations causing mild hemophilia A in Iceland detected by denaturing gradient gel electrophoresisS Jonsdottir, C Diamond, B Levinson, et al.
American Journal of Human Genetics|May 1, 1995
Wilson disease in Iceland: a clinical and genetic studyG R Thomas, O Jensson, G Gudmundsson, et al.
The New England Journal of Medicine|December 13, 1984
Abnormal metabolism of gamma-trace alkaline microprotein. The basic defect in hereditary cerebral hemorrhage with amyloidosisA Grubb, O Jensson, G Gudmundsson, et al.
Journal of Medical Genetics|April 1, 1988
A family showing apparent X linked inheritance of both anencephaly and spina bifidaO Jensson, A Arnason, H Gunnarsdottir, et al.
Acta Medica Scandinavica|January 1, 1982
Serum amyloid P-component and C-reactive protein in serum of healthy Icelanders and members of an Icelandic family with macroglobulinaemiaO Jensson, O G Björnsson, A Arnason, et al.
Acta Medica Scandinavica|January 1, 1978
Macroglobulinaemia in an Icelandic familyO G Björnsson, A Arnason, S Gudmunosson, et al.
Scandinavian Journal of Immunology|September 1, 1990
The first Icelandic family with X-linked agammaglobulinaemia: studies of genetic markers and immune functionL Thorsteinsson, H M Ogmundsdóttir, A Sigfússon, et al.
Lancet (London, England)|September 10, 1988
Mutation in cystatin C gene causes hereditary brain haemorrhageA Palsdottir, M Abrahamson, L Thorsteinsson, et al.
Pageof 11