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O Jensson

Showing results (61-70 of 102) with videos related to

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Acta Neurologica Scandinavica|August 1, 1987
Hereditary cystatin C (gamma-trace) amyloid angiopathy of the CNS causing cerebral hemorrhageO Jensson, G Gudmundsson, A Arnason, et al.
Progress in Clinical and Biological Research|January 1, 1983
Epidemiology of delta infection in ScandinaviaB G Hansson, G Norkrans, M Weibull, et al.
Nature|March 5, 1987
Linkage of an X-chromosome cleft palate geneG E Moore, A Ivens, J Chambers, et al.
Journal of Immunogenetics|August 1, 1979
Anti-tissue antibodies and immunoglobulin levels in relation to HLA and other markers in Icelandic familiesN Williamson, J H Edwards, K Monk, et al.
European Journal of Human Genetics : EJHG|March 12, 2021
Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiencyHrafnhildur L Runolfsdottir, John A Sayer, Olafur S Indridason, et al.
BMC Medical Genetics|October 3, 2017
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sistersGudny A Arnadottir, Brynjar O Jensson, Sigurdur E Marelsson, et al.
Journal of the American Heart Association|July 14, 2023
Screening for Rare Coding Variants That Associate With the QTc Interval in IcelandGardar Sveinbjornsson, Bara D Benediktsdottir, Gunnlaugur Sigfusson, et al.
BMC Medical Genetics|November 16, 2017
COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPABrynjar O Jensson, Sif Hansdottir, Gudny A Arnadottir, et al.
NPJ Parkinson'S Disease|August 15, 2024
Loss-of-function variants in ITSN1 confer high risk of Parkinson's diseaseAstros Th Skuladottir, Vinicius Tragante, Gardar Sveinbjornsson, et al.
Nature Communications|February 4, 2016
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenaseRagnar P Kristjansson, Asmundur Oddsson, Hannes Helgason, et al.
Pageof 11

Showing results (61-70 of 102) with videos related to

Sort By:
Pageof 11
Acta Neurologica Scandinavica|August 1, 1987
Hereditary cystatin C (gamma-trace) amyloid angiopathy of the CNS causing cerebral hemorrhageO Jensson, G Gudmundsson, A Arnason, et al.
Progress in Clinical and Biological Research|January 1, 1983
Epidemiology of delta infection in ScandinaviaB G Hansson, G Norkrans, M Weibull, et al.
Nature|March 5, 1987
Linkage of an X-chromosome cleft palate geneG E Moore, A Ivens, J Chambers, et al.
Journal of Immunogenetics|August 1, 1979
Anti-tissue antibodies and immunoglobulin levels in relation to HLA and other markers in Icelandic familiesN Williamson, J H Edwards, K Monk, et al.
European Journal of Human Genetics : EJHG|March 12, 2021
Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiencyHrafnhildur L Runolfsdottir, John A Sayer, Olafur S Indridason, et al.
BMC Medical Genetics|October 3, 2017
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sistersGudny A Arnadottir, Brynjar O Jensson, Sigurdur E Marelsson, et al.
Journal of the American Heart Association|July 14, 2023
Screening for Rare Coding Variants That Associate With the QTc Interval in IcelandGardar Sveinbjornsson, Bara D Benediktsdottir, Gunnlaugur Sigfusson, et al.
BMC Medical Genetics|November 16, 2017
COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPABrynjar O Jensson, Sif Hansdottir, Gudny A Arnadottir, et al.
NPJ Parkinson'S Disease|August 15, 2024
Loss-of-function variants in ITSN1 confer high risk of Parkinson's diseaseAstros Th Skuladottir, Vinicius Tragante, Gardar Sveinbjornsson, et al.
Nature Communications|February 4, 2016
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenaseRagnar P Kristjansson, Asmundur Oddsson, Hannes Helgason, et al.
Pageof 11