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The INTROL Cystic Fibrosis cystic fibrosis (sĭs`tĭk fībrō`sĭs), inherited disorder of the exocrine glands (see gland), affecting children and young people; median survival is 25 years in females and 30 years in males.  Panel I Control is intended for use as a control product to monitor the analytical performance of the extraction, amplification amplification /am·pli·fi·ca·tion/ (33000) (am?pli-fi-ka´shun) the process of making larger, such as the increase of an auditory stimulus, as a means of improving its perception. , and detection of test systems used in the qualitative measurement of the cystic-fibrosis transmembrane transmembrane /trans·mem·brane/ (trans-mem´bran) extending across a membrane, usually referring to a protein subunit that is exposed on both sides of a cell membrane.

trans·mem·brane
adj.
 conductance regulator (CFTR) gene.

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Title Annotation:Cystic-fibrosis products
Publication:Medical Laboratory Observer
Date:Jul 1, 2008
Words:53
Previous Article:Direct sequence analysis.(Cystic-fibrosis products)
Next Article:Comprehensive test.(Cystic-fibrosis products)
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