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Publications by M P Audrezet
Association of 1078 Del T Cystic Fibrosis Mutation With Severe Disease.
Journal of Medical Genetics
Genetics
A Mutation in Exon 7 of the CFTR Gene Is Common in the Western Part of France.
Journal of Medical Genetics
Genetics
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The Cystic Fibrosis F508del Mutation in Crohn's Disease
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Sleep Quality and Daytime Function in Adults With Cystic Fibrosis and Severe Lung Disease
European Respiratory Journal
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Cystic Fibrosis Gene Mutation in Two Sisters With Mild Disease and Normal Sweat Electrolyte Levels
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Clinical Features of Cystic Fibrosis Patients With Chronic Liver Disease in Turkish National Cystic Fibrosis Registry
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Origins of Cystic Fibrosis Lung Disease
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A Missense Cystic Fibrosis Transmembrane Conductance Regulator Mutation With Variable Phenotype
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Crohnʼs Disease in Cystic Fibrosis
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Intestinal Disease in Cystic Fibrosis.
Archives of Disease in Childhood
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Studies on Cystic Fibrosis Using Isoelectric Focusing. IV. Distinction Between Ciliary Dyskinesia Activity in Cystic Fibrosis and Asthmatic Sera and Association of Cystic Fibrosis Protein With the Activity in Cystic Fibrosis Serum
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