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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
M.G Zaahl, L du Plessis, L Warnich, M.J Kotze, S.W MooreVolume:
17
Year:
2003
Language:
english
DOI:
10.1016/s0890-8508(03)00003-3
File:
PDF, 102 KB
english, 2003