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Forensic Science International|December 20, 2011
Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathyM K Larsen, P H Nissen, K E Berge, et al.
Journal of Internal Medicine|February 13, 2008
Characterization of novel mutations in the catalytic domain of the PCSK9 geneJ Cameron, O L Holla, J K Laerdahl, et al.
International Journal of Legal Medicine|January 7, 2012
Postmortem genetic testing of the ryanodine receptor 2 (RYR2) gene in a cohort of sudden unexplained death casesM K Larsen, K E Berge, T P Leren, et al.
Science (New York, N.Y.)|December 2, 2000
Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transportersK E Berge, H Tian, G A Graf, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|August 30, 2008
Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriersK E Berge, K H Haugaa, A Früh, et al.
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