Arthrogryposis multiplex congenita distal type II associated with facial abnormality, renal abnormality, Polydactyly and Hirschprung's disease

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dc.contributor.authorSooriyabandara, S.
dc.contributor.authorAluwihare, A.P.R.
dc.date.accessioned2016-01-14T09:45:13Z
dc.date.available2016-01-14T09:45:13Z
dc.date.issued2001
dc.identifier.citationThe Ceylon Medical Journal, 46(4)pp.156-157
dc.identifier.urihttps://dl.nsf.gov.lk/handle/1/21779
dc.titleArthrogryposis multiplex congenita distal type II associated with facial abnormality, renal abnormality, Polydactyly and Hirschprung's disease
dc.typeArticle

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