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O Jensson

Showing results (11-20 of 102) with videos related to

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Forensic Science International|August 1, 1983
An unusual Rhesus haplotype, --D--, in IcelandS Olafsdóttir, O Jensson, G Thordarson, et al.
Nucleic Acids Research|March 11, 1987
Bgl II polymorphic site upstream to the human complement component C4A geneA Palsdottir, R Fossdal, O Jensson, et al.
Human Genetics|July 1, 1987
Gene organization of haplotypes expressing two different C4A allotypesA Palsdottir, A Arnason, R Fossdal, et al.
Clinical Genetics|November 1, 1989
The saga of cystatin C gene mutation causing amyloid angiopathy and brain hemorrhage--clinical genetics in IcelandO Jensson, A Palsdottir, L Thorsteinsson, et al.
Human Molecular Genetics|March 1, 1995
Mapping the locus of atrophia areata, a helicoid peripapillary chorioretinal degeneration with autosomal dominant inheritance, to chromosome 11p15R Fossdal, L Magnússon, J L Weber, et al.
Acta Medica Scandinavica|January 1, 1977
Studies on the Pelger anomaly in IcelandO Jensson, K Arnason, G M Jóhannesson, et al.
The Journal of Experimental Medicine|August 1, 1983
Amyloid fibril in hereditary cerebral hemorrhage with amyloidosis (HCHWA) is related to the gastroentero-pancreatic neuroendocrine protein, gamma traceD H Cohen, H Feiner, O Jensson, et al.
Journal of Internal Medicine|May 1, 1994
Mild haemophilia A in Iceland: clinical genetic studies of three families with the same mutationO Jensson, S Stenbjerg Bernvil, S Jónsdóttir, et al.
Human Heredity|January 1, 1983
Gc subtypes in IcelandersS Karlsson, I Skaftadóttir, A Arnason, et al.
Human Genetics|June 1, 1992
Hereditary cystatin C amyloid angiopathy: identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysisM Abrahamson, S Jonsdottir, I Olafsson, et al.
Pageof 11

Showing results (11-20 of 102) with videos related to

Sort By:
Pageof 11
Forensic Science International|August 1, 1983
An unusual Rhesus haplotype, --D--, in IcelandS Olafsdóttir, O Jensson, G Thordarson, et al.
Nucleic Acids Research|March 11, 1987
Bgl II polymorphic site upstream to the human complement component C4A geneA Palsdottir, R Fossdal, O Jensson, et al.
Human Genetics|July 1, 1987
Gene organization of haplotypes expressing two different C4A allotypesA Palsdottir, A Arnason, R Fossdal, et al.
Clinical Genetics|November 1, 1989
The saga of cystatin C gene mutation causing amyloid angiopathy and brain hemorrhage--clinical genetics in IcelandO Jensson, A Palsdottir, L Thorsteinsson, et al.
Human Molecular Genetics|March 1, 1995
Mapping the locus of atrophia areata, a helicoid peripapillary chorioretinal degeneration with autosomal dominant inheritance, to chromosome 11p15R Fossdal, L Magnússon, J L Weber, et al.
Acta Medica Scandinavica|January 1, 1977
Studies on the Pelger anomaly in IcelandO Jensson, K Arnason, G M Jóhannesson, et al.
The Journal of Experimental Medicine|August 1, 1983
Amyloid fibril in hereditary cerebral hemorrhage with amyloidosis (HCHWA) is related to the gastroentero-pancreatic neuroendocrine protein, gamma traceD H Cohen, H Feiner, O Jensson, et al.
Journal of Internal Medicine|May 1, 1994
Mild haemophilia A in Iceland: clinical genetic studies of three families with the same mutationO Jensson, S Stenbjerg Bernvil, S Jónsdóttir, et al.
Human Heredity|January 1, 1983
Gc subtypes in IcelandersS Karlsson, I Skaftadóttir, A Arnason, et al.
Human Genetics|June 1, 1992
Hereditary cystatin C amyloid angiopathy: identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysisM Abrahamson, S Jonsdottir, I Olafsson, et al.
Pageof 11