Novel RET mutations in Hirschsprung's disease patients from the diverse South African population von Julies, M G, Moore, S W, Kotze, M J, du Plessis, L

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Mapping of novel regions of DNA gain and loss by comparative genomic hybridization in esophageal carcinoma in the Black and colored populations of South Africa von PLESSIS, L. D, DIETZSCH, E, SPELEMAN, F, VAN GELE, M, VAN ROY, N, VAN HELDEN, P, PARKER, M. I, MUGWANYA, D. K, DE GROOT, M, MARX, M. P, KOTZE, M. J

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Analysis of the NRAMP1 Gene Implicated in Iron Transport: Association with Multiple Sclerosis and Age Effects von Kotze, Maritha J., de Villiers, J.Nico P., Rooney, Roberta N., Grobbelaar, Johanna J., Mansvelt, Erna P.G., Bouwens, Christianne S.H., Carr, Jonathan, Stander, Ilse, du Plessis, Lana

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Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyria von De Villiers, J. Nico P., Kotze, Maritha J., Van Heerden, Carel J., Sadie, Annalene, Gardner, Helena F. J., Liebenberg, Juanita, Van Zyl, René, Du Plessis, Lana, Kimberg, Matti, Frank, Jorge, Warnich, Louise

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Familial hypercholesterolemia: potential diagnostic value of mutation screening in a pediatric population of South Africa von Kotze, Maritha J., Peeters, Armand V., Loubser, Odell, Theart, Leonora, du Plessis, Lana, Hayes, Vanessa M., de Jong, Greetje, de Villiers, J. Nico P., Lombard, Carl J., Hansen, Peter S., Raal, Frederick J.

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