Paul Brink
0000-0001-8538-5824
Stellenbosch University
91 papers found
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X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.
Polymerase chain reaction-based detection of MN blood group-specific sequences in the human genome
Identification of a new missense mutation at Arg403, a CpG mutation hotspot, in exon 13 of the β-myosin heavy chain gene in hypertrophic cardiomyopathy
Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population
Relevance of ancestral surname identification in pedigrees of Afrikaner families with familial hypercholesterolaemia
Linkage study of the low-density lipoprotein-receptor gene and cholesterol levels in an Afrikaner family. Quantitative genetics and identification of a minor founder effect
Familial hypercholesterolemia in South African Afrikaners
RFLP for the human LDL receptor gene (LDLR): Bst EII.
Plasma vitamin A, E, C and B6levels in myocardial infarction
Linkage disequilibrium between a marker on the low-density lipoprotein receptor and high cholesterol levels
A DNA polymorphism in the human low-density lipoprotein receptor gene
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