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K Sigvard Olsson

Showing results (1-10 of 7) with videos related to

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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|September 17, 2009
[Hemochromatosis]K Sigvard Olsson
Lakartidningen|February 25, 2016
[Was the boat packed with hemochromatosis?]K Sigvard Olsson
Haematologica|June 3, 2008
Comment to: Hepcidin: from discovery to differential diagnosis. Haematologica 2008; 93:90-7K Sigvard Olsson, Anders Norrby
European Journal of Haematology|October 11, 2007
The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype?K Sigvard Olsson, Bernd Ritter, Norbeth Hansson
European Journal of Haematology|November 17, 2009
HLA-A3-B14 and the origin of the haemochromatosis C282Y mutation: founder effects and recombination events during 12 generations in a Scandinavian family with major iron overloadK Sigvard Olsson, Bernd Ritter, Ruma Raha-Chowdhury
European Journal of Haematology|March 28, 2008
HLA haplotype map of river valley populations with hemochromatosis traced through five centuries in Central SwedenK Sigvard Olsson, Bernd Ritter, Norbeth Hansson, et al.
Hereditas|December 23, 2017
Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the <i>WHRN</i> and <i>TMC1</i> genesK Sigvard Olsson, Olof Wålinder, Ulf Jansson, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|September 17, 2009
[Hemochromatosis]K Sigvard Olsson
Lakartidningen|February 25, 2016
[Was the boat packed with hemochromatosis?]K Sigvard Olsson
Haematologica|June 3, 2008
Comment to: Hepcidin: from discovery to differential diagnosis. Haematologica 2008; 93:90-7K Sigvard Olsson, Anders Norrby
European Journal of Haematology|October 11, 2007
The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype?K Sigvard Olsson, Bernd Ritter, Norbeth Hansson
European Journal of Haematology|November 17, 2009
HLA-A3-B14 and the origin of the haemochromatosis C282Y mutation: founder effects and recombination events during 12 generations in a Scandinavian family with major iron overloadK Sigvard Olsson, Bernd Ritter, Ruma Raha-Chowdhury
European Journal of Haematology|March 28, 2008
HLA haplotype map of river valley populations with hemochromatosis traced through five centuries in Central SwedenK Sigvard Olsson, Bernd Ritter, Norbeth Hansson, et al.
Hereditas|December 23, 2017
Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the <i>WHRN</i> and <i>TMC1</i> genesK Sigvard Olsson, Olof Wålinder, Ulf Jansson, et al.
Pageof 1