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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Monique G. Zaahl

Department of Genetics

University of Stellenbosch

Stellenbosch

South Africa

[email]@sun.ac.za

Name/email consistency: low

 
 
 
 
 
 
 

Affiliations

  • Department of Genetics, University of Stellenbosch, Stellenbosch, South Africa. 2004 - 2006
  • MRC Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, United Kingdom. 2004
  • Division of Human Genetics, Faculty of Health Sciences, University of Stellenbosch, Tygerberg, South Africa. 2003

References

  1. The -237C-->T promoter polymorphism of the SLC11A1 gene is associated with a protective effect in relation to inflammatory bowel disease in the South African population. Zaahl, M.G., Winter, T.A., Warnich, L., Kotze, M.J. Int. J. Colorectal. Dis (2006) [Pubmed]
  2. Association of functional polymorphisms of SLC11A1 with risk of esophageal cancer in the South African Colored population. Zaahl, M.G., Warnich, L., Victor, T.C., Kotze, M.J. Cancer Genet. Cytogenet. (2005) [Pubmed]
  3. Analysis of the three common mutations in the CARD15 gene (R702W, G908R and 1007fs) in South African colored patients with inflammatory bowel disease. Zaahl, M.G., Winter, T., Warnich, L., Kotze, M.J. Mol. Cell. Probes (2005) [Pubmed]
  4. Expression of the SLC11A1 (NRAMP1) 5'-(GT)n repeat: opposite effect in the presence of -237C-->T. Zaahl, M.G., Robson, K.J., Warnich, L., Kotze, M.J. Blood Cells Mol. Dis. (2004) [Pubmed]
  5. Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload. Zaahl, M.G., Merryweather-Clarke, A.T., Kotze, M.J., van der Merwe, S., Warnich, L., Robson, K.J. Hum. Genet. (2004) [Pubmed]
  6. Significance of novel endothelin-B receptor gene polymorphisms in Hirschsprung's disease: predominance of a novel variant (561C/T) in patients with co-existing Down's syndrome. Zaahl, M.G., du Plessis, L., Warnich, L., Kotze, M.J., Moore, S.W. Mol. Cell. Probes (2003) [Pubmed]
 
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