Reduced lung function in cystic fibrosis: Primary or secondary phenotype?

Stephanie Davis, Felix Ratjen

Research output: Contribution to journalArticle

10 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)2-3
Number of pages2
JournalAmerican Journal of Respiratory and Critical Care Medicine
Volume178
Issue number1
DOIs
StatePublished - Jul 1 2008
Externally publishedYes

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Maximal Midexpiratory Flow Rate
Pseudomonas Infections
Respiratory Function Tests
Forced Expiratory Volume
Preschool Children
Cystic Fibrosis
Phenotype
Lung

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

Cite this

Reduced lung function in cystic fibrosis : Primary or secondary phenotype? / Davis, Stephanie; Ratjen, Felix.

In: American Journal of Respiratory and Critical Care Medicine, Vol. 178, No. 1, 01.07.2008, p. 2-3.

Research output: Contribution to journalArticle

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