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

Molecular and Cellular Probes - Tập 17 - Trang 49-54 - 2003
M.G Zaahl1,2, L du Plessis1, L Warnich2, M.J Kotze2,3, S.W Moore4
1Division of Human Genetics, Faculty of Health Sciences, University of Stellenbosch, Tygerberg, South Africa
2Department of Genetics, University of Stellenbosch, Private Bag X1, Matieland, Stellenbosch, South Africa
3Genecare Molecular Genetics, Christiaan Barnard Annexe, Cape Town, South Africa
4Division of Pediatric Surgery, Faculty of Health Sciences, University of Stellenbosch, Tygerberg, South Africa

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Molecular and Cellular Probes

Tập 17

49-54

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