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.

Simple item page
dc.contributor.authorZaahl MG
dc.contributor.authorDu Plessis L
dc.contributor.authorWarnich L
dc.contributor.authorKotze MJ
dc.contributor.authorMoore SW
dc.date.accessioned2013-01-23T14:11:31Z
dc.date.available2013-01-23T14:11:31Z
dc.date.issued2004
dc.descriptionAgriwetenskappe
dc.descriptionGenetika
dc.descriptionPlease help us populate SUNScholar with the post print version of this article. It can be e-mailed to: scholar@sun.ac.za
dc.identifier.citationMolecular and Cellular Probes
dc.identifier.urihttp://hdl.handle.net/10019.1/79081
dc.publisherACADEMIC PRESS LTD ELSEVIER SCIENCE LTD, 24-28 OVAL RD, LONDON, ENGLAND, NW17DX
dc.titleSignificance 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.
dc.typeJournal Articles (subsidised)
Files
Collections
2004 - Research Outputs