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Genomic medicine and risk prediction across the disease spectrum.
Kotze MJ, Lückhoff HK, Peeters AV, Baatjes K, Schoeman M, van der Merwe L, Grant KA, Fisher LR, van der Merwe N, Pretorius J, van Velden DP, Myburgh EJ, Pienaar FM, van Rensburg SJ, Yako YY, September AV, Moremi KE, Cronje FJ, Tiffin N, Bouwens CS, Bezuidenhout J, Apffelstaedt JP, Hough FS, Erasmus RT, Schneider JW. Kotze MJ, et al. Among authors: van der merwe n. Crit Rev Clin Lab Sci. 2015;52(3):120-37. doi: 10.3109/10408363.2014.997930. Epub 2015 Jan 19. Crit Rev Clin Lab Sci. 2015. PMID: 25597499 Review.
Globally Rare BRCA2 Variants With Founder Haplotypes in the South African Population: Implications for Point-of-Care Testing Based on a Single-Institution BRCA1/2 Next-Generation Sequencing Study.
Oosthuizen J, Kotze MJ, Van Der Merwe N, Myburgh EJ, Bester P, van der Merwe NC. Oosthuizen J, et al. Among authors: van der merwe n. Front Oncol. 2021 Feb 12;10:619469. doi: 10.3389/fonc.2020.619469. eCollection 2020. Front Oncol. 2021. PMID: 33643918 Free PMC article.