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American Journal of Respiratory and Critical Care Medicine|May 1, 1996
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic childrenL C Martinati, E Trabetti, A Casartelli, et al.Bone Marrow Transplantation|December 1, 1989
Bone marrow transplantation monitoring by DNA analysisP Gasparini, G Martinelli, E Trabetti, et al.Journal of Medical Genetics|August 1, 1992
Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung diseaseP Gasparini, G Borgo, G Mastella, et al.Matrix (Stuttgart, Germany)|March 1, 1990
Anomalous cysteine in type I collagen. Localisation by chemical cleavage of the protein using 2-nitro-5-thiocyanobenzoic acid and by mismatch analysis of cDNA heteroduplexesR Tenni, A Rossi, M Valli, et al.Human Genetics|September 1, 1990
Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF familiesG Novelli, P Gasparini, A Savoia, et al.European Journal of Pediatrics|December 1, 1993
Cystic fibrosis: the delta F508 mutation does not lead to an exceptionally severe phenotype. A cohort studyG Borgo, P Gasparini, A Bonizzato, 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.Journal of Medical Genetics|November 1, 1990
Pancreatic function and gene deletion F508 in cystic fibrosisG Borgo, G Mastella, P Gasparini, et al.Biochemistry|April 6, 1976
Characterization of the gamma subunits of the 7S nerve growth factor complexR W Stach, A C Server, P F Pignatti, et al.Recenti Progressi in Medicina|January 1, 1990
Search of HIV DNA by polymerase chain reaction in the urine sediments of seropositive individualsP Gasparini, A Savoia, P F Pignatti, et al.Pageof 18