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Human Genetics|June 29, 1976
Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine replaced by threonine at position 75 )E 19) of the gamma chainG Ricco, U Mazza, R M Turi, et al.Human Heredity|January 1, 1990
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian populationP Gasparini, E Trabetti, A Savoia, et al.Molecular Syndromology|August 3, 2012
Identification of a New Mutation (L46P) in the Human NOG Gene in an Italian Patient with Symphalangism SyndromeE Athanasakis, X Biarnés, M T Bonati, et al.American Journal of Respiratory Cell and Molecular Biology|March 1, 1990
The cystic fibrosis gene is not likely to be involved in chronic obstructive pulmonary diseaseP Gasparini, A Savoia, M Luisetti, et al.Journal of Inherited Metabolic Disease|January 1, 1989
RFLPs of the phenylalanine hydroxylase gene in the Italian populationI Dianzani, L Farinasso, P Fortina, et al.European Journal of Pediatrics|January 28, 2003
Diagnosis of juvenile hemochromatosis in an 11-year-old child combining genetic analysis and non-invasive liver iron quantitationM De Gobbi, R Caruso, F Daraio, et al.The EMBO Journal|November 1, 1984
A molecular study of a family with Greek hereditary persistence of fetal hemoglobin and beta-thalassemiaB Giglioni, C Casini, R Mantovani, et al.British Journal of Haematology|August 1, 1991
A newly-characterized alpha-thalassaemia-1 deletion removes the entire alpha-like globin gene cluster in an Italian familyP Fortina, I Dianzani, A Serra, et al.British Journal of Haematology|October 1, 1982
G gamma and a gamma globin chain synthesis in bone marrow and peripheral blood of beta-thalassaemia homozygotesG Saglio, C Camaschella, A Guerrasio, et al.Journal of Neurology|October 1, 1994
The myelin basic protein gene is not a major susceptibility locus for multiple sclerosis in Italian patientsM Eoli, M Pandolfo, C Milanese, et al.Pageof 25