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pubmed-article:16243854pubmed:abstractTextTo investigate the immunoreactive trypsinogen (IRT) values above the usual 99th centile laboratory cut-off and determine the value of offering further testing to those infants with a markedly elevated IRT but no cystic fibrosis transmembrane regulator (CFTR) gene mutation identified by the screening programme.lld:pubmed
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pubmed-article:16243854pubmed:articleTitleMarkedly elevated neonatal immunoreactive trypsinogen levels in the absence of cystic fibrosis gene mutations is not an indication for further testing.lld:pubmed
pubmed-article:16243854pubmed:affiliationDepartment of Respiratory Medicine, Royal Children's Hospital, Parkville, Victoria, Australia. john.massie@rch.org.aulld:pubmed
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