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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1990 | 1 |
1992 | 2 |
1993 | 1 |
2024 | 0 |
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Page 1
Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction.
Hum Genet. 1993 Apr;91(3):299-300. doi: 10.1007/BF00218280.
Hum Genet. 1993.
PMID: 8478017
No abstract available.
Familial defective apolipoprotein B-100: a single mutation that causes hypercholesterolemia and premature coronary artery disease.
Tybjaerg-Hansen A, Humphries SE.
Tybjaerg-Hansen A, et al.
Atherosclerosis. 1992 Oct;96(2-3):91-107. doi: 10.1016/0021-9150(92)90056-m.
Atherosclerosis. 1992.
PMID: 1466657
Review.
Item in Clipboard
Familial defective apolipoprotein B-100: a common cause of primary hypercholesterolemia.
Rauh G, Keller C, Schuster H, Wolfram G, Zöllner N.
Rauh G, et al.
Clin Investig. 1992 Jan;70(1):77-84. doi: 10.1007/BF00422946.
Clin Investig. 1992.
PMID: 1600334
Review.
Item in Clipboard
Absence of familial defective apolipoprotein B-100 in Finnish patients with elevated serum cholesterol.
Hämäläinen T, Palotie A, Aalto-Setälä K, Kontula K, Tikkanen MJ.
Hämäläinen T, et al.
Atherosclerosis. 1990 Jun;82(3):177-83. doi: 10.1016/0021-9150(90)90038-k.
Atherosclerosis. 1990.
PMID: 2375782
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