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Markedly elevated neonatal immunoreactive trypsinogen levels in the absence of cystic fibrosis gene mutations is not an indication for further testing
AIMS: To 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 scr...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2065933/ https://ncbi.nlm.nih.gov/pubmed/16243854 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/adc.2005.081349 |
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