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Human Mutation|April 29, 1998
Identification of a novel mutation (S13F) in the CFTR gene in a CF patient of Sardinian originG B Leoni, S Pitzalis, R Tonelli, et al.Recenti Progressi in Medicina|April 1, 1992
Prenatal diagnosis of inherited hemoglobinopathiesA Cao, G B Leoni, R Sardu, et al.Human Genetics|September 1, 1990
Molecular bases for cystic fibrosis in the Sardinian populationG B Leoni, C Rosatelli, R Sardu, et al.Journal of Medical Genetics|February 1, 1987
Beta thalassaemia mutations in Sardinians: implications for prenatal diagnosisC Rosatelli, G B Leoni, T Tuveri, et al.Acta Haematologica|January 1, 1991
Molecular basis of beta-thalassemia intermedia in a southern Italian region (Puglia)G B Leoni, C Rosatelli, A Vitucci, et al.Haematologica|March 1, 1992
Beta-globin haplotype and XmnI polymorphism at position G (gamma)-158 and HbF production in Fanconi's anemiaM C Rosatelli, C Altay, R Oner, et al.British Journal of Haematology|February 15, 2002
Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemiaR Galanello, S Piras, S Barella, et al.International Endodontic Journal|December 31, 2015
Evaluation of bond strength in single-cone fillings of canals with different cross-sectionsR D Pereira, M Brito-Júnior, G B Leoni, et al.The Journal of Pediatrics|August 1, 1995
A specific cystic fibrosis mutation (T3381) associated with the phenotype of isolated hypotonic dehydrationG B Leoni, S Pitzalis, R Podda, et al.American Journal of Hematology|January 1, 1992
Heterozygous beta-thalassemia: relationship between the hematological phenotype and the type of beta-thalassemia mutationC Rosatelli, G B Leoni, T Tuveri, et al.Pageof 2