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Human Molecular Genetics|April 1, 1995
Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasisP F Pignatti, C Bombieri, C Marigo, et al.Molecular and Cellular Probes|April 1, 1995
Homozygosity for a novel splice site mutation (2790-2 A--->G) preceding exon 15 of the CFTR gene in a cystic fibrosis patient of North-East Italian descentC Marigo, C Bombieri, L Bisceglia, et al.Stem Cell Research & Therapy|April 12, 2025
The bone microenvironment: new insights into the role of stem cells and cell communication in bone regenerationL Dalle Carbonare, M Cominacini, E Trabetti, et al.Human Genetics|January 28, 1999
Complete mutational screening of the CFTR gene in 120 patients with pulmonary diseaseC Bombieri, M Benetazzo, A Saccomani, et al.Respiratory Medicine|October 30, 1999
alpha 1-antitrypsin TAQ I polymorphism and alpha 1-antichymotrypsin mutations in patients with obstructive pulmonary diseaseM G Benetazzo, L S Gilè, C Bombieri, et al.European Journal of Human Genetics : EJHG|September 12, 2000
Increased frequency of CFTR gene mutations in sarcoidosis: a case/control association studyC Bombieri, M Luisetti, F Belpinati, et al.Human Genetics|April 1, 1995
Analysis of the complete coding region of the CFTR gene in a cohort of CF patients from north-eastern Italy: identification of 90% of the mutationsA Bonizzato, L Bisceglia, C Marigo, et al.Human Mutation|January 1, 1993
Screening of 62 mutations in a cohort of cystic fibrosis patients from north eastern Italy: their incidence and clinical features of defined genotypesP Gasparini, C Marigo, G Bisceglia, et al.British Journal of Haematology|December 19, 1998
The haemochromatosis mutations do not modify the clinical picture of thalassaemia major in patients regularly transfused and chelatedC Borgna-Pignatti, A Solinas, C Bombieri, et al.Pageof 2