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R Fossdal

Showing results (1-10 of 15) with videos related to

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Human Genetics|July 1, 1987
Gene organization of haplotypes expressing two different C4A allotypesA Palsdottir, A Arnason, R Fossdal, 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 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.
Laeknabladid|March 27, 2009
[Autosomal dominant polycystic kidney disease in Iceland - genetic study.]R Fossdal, M Bodvarsson, P Asmundsson, 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.
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.
Human Genetics|July 1, 1993
Icelandic families with autosomal dominant polycystic kidney disease: families unlinked to chromosome 16p13.3 revealed by linkage analysisR Fossdal, M Böthvarsson, P Asmundsson, et al.
Annals of the Rheumatic Diseases|November 3, 1998
A study of the association of HLA DR, DQ, and complement C4 alleles with systemic lupus erythematosus in IcelandK Steinsson, S Jónsdóttir, G J Arason, et al.
The Journal of Rheumatology|October 1, 1995
A study of the major histocompatibility complex in a Caucasian family with multiple cases of systemic lupus erythematosus: association with the C4AQ0 phenotypeK Steinsson, A Arnason, K Erlendsson, et al.
Genes and Immunity|December 4, 2003
Genome-wide TDT analysis in a localized population with a high prevalence of multiple sclerosis indicates the importance of a region on chromosome 14qV Giedraitis, H Modin, M Callander, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Human Genetics|July 1, 1987
Gene organization of haplotypes expressing two different C4A allotypesA Palsdottir, A Arnason, R Fossdal, 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 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.
Laeknabladid|March 27, 2009
[Autosomal dominant polycystic kidney disease in Iceland - genetic study.]R Fossdal, M Bodvarsson, P Asmundsson, 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.
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.
Human Genetics|July 1, 1993
Icelandic families with autosomal dominant polycystic kidney disease: families unlinked to chromosome 16p13.3 revealed by linkage analysisR Fossdal, M Böthvarsson, P Asmundsson, et al.
Annals of the Rheumatic Diseases|November 3, 1998
A study of the association of HLA DR, DQ, and complement C4 alleles with systemic lupus erythematosus in IcelandK Steinsson, S Jónsdóttir, G J Arason, et al.
The Journal of Rheumatology|October 1, 1995
A study of the major histocompatibility complex in a Caucasian family with multiple cases of systemic lupus erythematosus: association with the C4AQ0 phenotypeK Steinsson, A Arnason, K Erlendsson, et al.
Genes and Immunity|December 4, 2003
Genome-wide TDT analysis in a localized population with a high prevalence of multiple sclerosis indicates the importance of a region on chromosome 14qV Giedraitis, H Modin, M Callander, et al.
Pageof 2