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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
August 10, 1997
[Expectations of listed patients]
K S Bakken
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
September 30, 1996
[The trial with assigned physicians]
K S Bakken
Human Genetics
|
March 7, 1998
Screening for mutations of the apolipoprotein B gene causing hypocholesterolemia
T P Leren, K S Bakken, V Hoel, et al.
Journal of Lipid Research
|
January 1, 1997
Heterozygosity for apolipoprotein A-I(R160L)Oslo is associated with low levels of high density lipoprotein cholesterol and HDL-subclass LpA-I/A-II but normal levels of HDL-subclass LpA-I
T P Leren, K S Bakken, U Daum, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
February 20, 1997
[Application of gene technology in the diagnosis of familial hypercholesterolemia]
T P Leren, K S Bakken, O K Rødningen, et al.
Journal of Internal Medicine
|
March 1, 1997
Molecular genetics of familial hypercholesterolaemia in Norway
T P Leren, S Tonstad, K E Gundersen, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
August 10, 1997
[Expectations of listed patients]
K S Bakken
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
September 30, 1996
[The trial with assigned physicians]
K S Bakken
Human Genetics
|
March 7, 1998
Screening for mutations of the apolipoprotein B gene causing hypocholesterolemia
T P Leren, K S Bakken, V Hoel, et al.
Journal of Lipid Research
|
January 1, 1997
Heterozygosity for apolipoprotein A-I(R160L)Oslo is associated with low levels of high density lipoprotein cholesterol and HDL-subclass LpA-I/A-II but normal levels of HDL-subclass LpA-I
T P Leren, K S Bakken, U Daum, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
February 20, 1997
[Application of gene technology in the diagnosis of familial hypercholesterolemia]
T P Leren, K S Bakken, O K Rødningen, et al.
Journal of Internal Medicine
|
March 1, 1997
Molecular genetics of familial hypercholesterolaemia in Norway
T P Leren, S Tonstad, K E Gundersen, et al.
Page
of 1