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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/34061
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dc.contributor.authorCouper, R.-
dc.contributor.authorBelli, D.-
dc.contributor.authorDurie, P.-
dc.contributor.authorGaskin, K.-
dc.contributor.authorSarles, J.-
dc.contributor.authorWerlin, S.-
dc.date.issued2002-
dc.identifier.citationJournal of Pediatric Gastroenterology and Nutrition, 2002; 35(2):s213-s223-
dc.identifier.issn0277-2116-
dc.identifier.issn1536-4801-
dc.identifier.urihttp://hdl.handle.net/2440/34061-
dc.description© 2002 Lippincott Williams & Wilkins, Inc.-
dc.description.statementofresponsibilityRichard Couper; Dominique Belli; Peter Durie; Kevin Gaskin; Jacques Sarles; Steven Werlin-
dc.language.isoen-
dc.publisherLippincott Williams & Wilkins-
dc.source.urihttp://jpgn.org/pt/re/jpgn/fulltext.00005176-200208002-00020.htm-
dc.subjectHumans-
dc.subjectPancreatic Diseases-
dc.subjectCystic Fibrosis-
dc.subjectDiagnosis, Differential-
dc.subjectGastroenterology-
dc.subjectResearch-
dc.subjectChild-
dc.subjectSocieties, Medical-
dc.subjectPractice Guidelines as Topic-
dc.subjectChild Nutritional Physiological Phenomena-
dc.titlePancreatic disorders and cystic fibrosis: Working Group Report of the First World Congress of Pediatric Gastroenterology, Hepatology, and Nutrition-
dc.typeJournal article-
dc.identifier.doi10.1097/00005176-200208002-00020-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest
Paediatrics publications

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