Search Results - "Benetazzo, M G"

High Frequency of Cystic Fibrosis Transmembrane Regulator Mutation L997F in Patients with Recurrent Idiopathic Pancreatitis and in Newborns with Hypertrypsinemia by Gomez Lira, M., Benetazzo, M.G., Marzari, M.G., Bombieri, C., Belpinati, F., Castellani, C., Cavallini, G.C., Mastella, G., Pignatti, P.F.

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Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in neonatal hypertrypsinaemia with normal sweat test by CASTELLANI, CARLO, BENETAZZO, MARIA GIOVANNA, TAMANINI, ANNA, BEGNINI, ANGELA, MASTELLA, GIANNI, PIGNATTI, PIERFRANCO

“…A DNA polymorphic sequence of five thymines in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which is very commonly involved…”
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Cystic Fibrosis Mutations in Heterozygous Newborns with Hypertrypsinemia and Low Sweat Chloride by Castellani, C., Benetazzo, M.G., Bonizzato, A., Pignatti, P.F., Mastella, G.

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α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease by Benetazzo, M.G., Gilè, L.S., Bombieri, C., Malerba, G., Massobrio, M., Pignatti, P.F., Luisetti, M.

“…Obstructive pulmonary disease is a multifactorial condition deriving from the interaction of environmental and genetic factors. From biochemical knowledge of…”
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Genetics of chronic obstructive pulmonary disease and disseminated bronchiectasis by Luisetti, M, Gilé, L S, Bombieri, C, Benetazzo, M G, Pignatti, P F

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alpha 1-antitrypsin TAQ I polymorphism and alpha 1-antichymotrypsin mutations in patients with obstructive pulmonary disease by Benetazzo, M G, Gilè, L S, Bombieri, C, Malerba, G, Massobrio, M, Pignatti, P F, Luisetti, M

“…Obstructive pulmonary disease is a multifactorial condition deriving from the interaction of environmental and genetic factors. From biochemical knowledge of…”
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