Authors: Gebhardt, GS Scholtz, CL Hillermann, R Odendaal, HJ

Citation: Gs. Gebhardt et al., Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not withintrauterine growth restriction, EUR J OB GY, 97(2), 2001, pp. 174-177

Authors: Grobbelaar, JJ Fortuin, R Scholtz, CL Zikind, A Langenhoven, E Wyllie, AH Bubb, VJ Kotze, MJ

Citation: Jj. Grobbelaar et al., Familial adenomatous polyposis coli in South Africa - Molecular basis and diagnosis, S AFR MED J, 90(7), 2000, pp. 715-719

Authors: Scholtz, CL Lingenhel, A Hillermann, R Stander, IA Kriek, JA Marais, MP Odendaal, HJ Kraft, HG Utermann, G Kotze, MJ

Citation: Cl. Scholtz et al., Lipoprotein(A) determination and risk of cardiovascular disease in South African patients with familial hypercholesterolaemia, S AFR MED J, 90(4), 2000, pp. 374-378

Authors: Thiart, R Scholtz, CL Vergotine, J Hoogendijk, CF de Villiers, JNP Nissen, H Brusgaard, K Gaffney, D Hoffs, MS Vermaak, WJH Kotze, MJ

Citation: R. Thiart et al., Predominance of a 6 bp deletion in exon 2 of the LDL receptor gene in Africans with familial hypercholesterolaemia, J MED GENET, 37(7), 2000, pp. 514-519

Authors: Scholtz, CL Peeters, AV Hoogendijk, CF Thiart, R de Villiers, JNP Hillermann, R Liu, JW Marais, AD Kotze, MJ

Citation: Cl. Scholtz et al., Mutation-59c -> t in repeat 2 of the LDL receptor promoter: reduction in transcriptional activity and possible allelic interaction in a South Africanfamily with familial hypercholesterolaemia, HUM MOL GEN, 8(11), 1999, pp. 2025-2030

Authors: Loubser, O Marais, AD Kotze, MJ Godenir, N Thiart, R Scholtz, CL de Villiers, JNP Hillermann, R Firth, JC Weich, HFH Maritz, F Jones, S van der Westhuyzen, DR

Citation: O. Loubser et al., Founder mutations in the LDL receptor gene contribute significantly to thefamilial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry, CLIN GENET, 55(5), 1999, pp. 340-345