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Annals of Hematology|February 1, 1996
Analysis of microsatellite instability in chronic lymphoproliferative disordersG Volpe, B Gamberi, C Pastore, et al.
Blood|May 15, 1989
The homozygous state of G to A--117A gamma hereditary persistence of fetal hemoglobinC Camaschella, L Oggiano, M Sampietro, et al.
Blood|June 1, 1994
Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemiaP Fortina, T Parrella, M Sartore, et al.
Breast Cancer Research and Treatment|May 1, 1988
Distribution of Ha-RAS-1 proto-oncogene alleles in breast cancer patients and in a control populationG Saglio, C Camaschella, M Giai, et al.
Annales De Genetique|January 1, 1997
A recombination event close to HFE gene in hereditary hemochromatosisA Roetto, L Sbaiz, S Bosio, et al.
European Journal of Clinical Pharmacology|January 1, 1982
Dipyridamole treatment in chronic obstructive airways disease: effect on platelet regeneration timeE Tremoli, L Bertoli, R Merlini, et al.
Acta Cardiologica|January 1, 1984
Can pulmonary hypertension be predicted by non-invasive approach? Echocardiographic and haemodynamic studyL Bertoli, G Rizzato, R Merlini, et al.
Human Genetics|May 1, 1988
A frequent A gamma-hereditary persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with beta-thalassemiaS Ottolenghi, C Camaschella, P Comi, et al.
British Journal of Haematology|January 1, 1980
gamma chain composition in five Italian newborns heterozygous for Hb F Malta G gamma-117 His leads to ArgU Mazza, T Meloni, O David, et al.
British Journal of Haematology|May 1, 1987
A benign form of thalassaemia intermedia may be determined by the interaction of triplicated alpha locus and heterozygous beta-thalassaemiaC Camaschella, M T Bertero, A Serra, et al.
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