CLINICAL SCORING SYSTEMS IN CYSTIC FIBROSIS-WHAT ARE THE OPTIONS FOR DEVELOPING COUNTRIES? (LETTER)

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MORROW BRENDA MAY

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Journal Paper

Paper Information

Journal: Journal of Comprehensive Pediatrics Year:2013 | Volume:3 | Issue:5 Page(s): 205-207

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Information Journal Paper

Title

CLINICAL SCORING SYSTEMS IN CYSTIC FIBROSIS-WHAT ARE THE OPTIONS FOR DEVELOPING COUNTRIES? (LETTER)

Author(s)

MORROW BRENDA MAY | Issue Writer Certificate

Keywords

CYSTIC FIBROSIS

SHWACHMAN

Abstract

CYSTIC FIBROSIS (CF) is recognized as a serious, life-limiting autosomal recessive inherited condition, affecting multiple organs. Improvements in both diagnosis and management of CF has led to the recognition of a range of phenotypes, from mild to severe, with varying rates of disease progression.

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APA: Copy

MORROW, BRENDA MAY. (2013). CLINICAL SCORING SYSTEMS IN CYSTIC FIBROSIS-WHAT ARE THE OPTIONS FOR DEVELOPING COUNTRIES? (LETTER). JOURNAL OF COMPREHENSIVE PEDIATRICS, 3(5), 205-207. SID. https://sid.ir/paper/339417/en

Vancouver: Copy

MORROW BRENDA MAY. CLINICAL SCORING SYSTEMS IN CYSTIC FIBROSIS-WHAT ARE THE OPTIONS FOR DEVELOPING COUNTRIES? (LETTER). JOURNAL OF COMPREHENSIVE PEDIATRICS[Internet]. 2013;3(5):205-207. Available from: https://sid.ir/paper/339417/en

IEEE: Copy

BRENDA MAY MORROW, “CLINICAL SCORING SYSTEMS IN CYSTIC FIBROSIS-WHAT ARE THE OPTIONS FOR DEVELOPING COUNTRIES? (LETTER),” JOURNAL OF COMPREHENSIVE PEDIATRICS, vol. 3, no. 5, pp. 205–207, 2013, [Online]. Available: https://sid.ir/paper/339417/en

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