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A common Lithuanian mutation causing familial hypercholesterolemia in Ashkenazi Jews. [electronic resource] by
- Meiner, V
- Landsberger, D
- Berkman, N
- Reshef, A
- Segal, P
- Seftel, H C
- van der Westhuyzen, D R
- Jeenah, M S
- Coetzee, G A
- Leitersdorf, E
Producer: 19910906
In:
American journal of human genetics vol. 49
Availability: No items available.
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A 3-basepair deletion in repeat 1 of the LDL receptor promoter reduces transcriptional activity in a South African Pedi. [electronic resource] by
- Peeters, A V
- Kotze, M J
- Scholtz, C L
- De Waal, L F
- Rubinsztein, D C
- Coetzee, G A
- Zuliani, G
- Streiff, R
- Liu, J
- van der Westhuyzen, D R
Producer: 19980828
In:
Journal of lipid research vol. 39
Availability: No items available.
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73.
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Phenotypic variation among familial hypercholesterolemics heterozygous for either one of two Afrikaner founder LDL receptor mutations. [electronic resource] by
- Kotze, M J
- De Villiers, W J
- Steyn, K
- Kriek, J A
- Marais, A D
- Langenhoven, E
- Herbert, J S
- Graadt Van Roggen, J F
- Van der Westhuyzen, D R
- Coetzee, G A
Producer: 19931105
In:
Arteriosclerosis and thrombosis : a journal of vascular biology vol. 13
Availability: No items available.
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74.
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Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry. [electronic resource] by
- Loubser, O
- Marais, A D
- Kotze, M J
- Godenir, N
- Thiart, R
- Scholtz, C L
- de Villiers, J N
- Hillermann, R
- Firth, J C
- Weich, H F
- Maritz, F
- Jones, S
- van der Westhuyzen, D R
Producer: 19990824
In:
Clinical genetics vol. 55
Availability: No items available.
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