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Comment
. 2007 Oct;92(10):831-2.
doi: 10.1136/adc.2007.120311.

What and when to collect from infants with cystic fibrosis

Iolo Doull  1
Affiliations
Comment

What and when to collect from infants with cystic fibrosis

Iolo Doull. Arch Dis Child. 2007 Oct.

Abstract

Perspective on the papers by Cipolli et al and Hilliard et al (see pages 842 and 898)

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Conflict of interest statement

Competing interests: None.

Comment on

References

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    1. Hilliard T N, Sukhani S, Francis J.et al Bronchoscopy following diagnosis with cystic fibrosis. Arch Dis Child 200792898–899. - PMC - PubMed
    1. Welsh M J, Smith A E. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Cell 1993731251–1254. - PubMed
    1. McKone E F, Emerson S S, Edwards K L.et al Effect of genotype on phenotype and mortality in cystic fibrosis: a retrospective cohort study. Lancet 20033611671–1676. - PubMed
    1. FitzSimmons S C.Cystic Fibrosis Foundation Patient Registry 1995: Annual data report. Bethesda, MD: Cystic Fibrosis Foundation, August 1996