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Journal of Clinical Pathology|October 1, 1980
Chronic liver disease in transfusion-dependent thalassaemia: hepatitis B virus marker studiesS De Virgiliis, G Fiorelli, S Fargion, et al.Lancet (London, England)|February 2, 1985
Prenatal diagnosis of beta-thalassaemia with the synthetic-oligomer techniqueC Rosatelli, A M Falchi, T Tuveri, et al.Journal of Drug Targeting|April 10, 2003
In vitro and in vivo transfection of melanoma cells B16-F10 mediated by cholesterol-based cationic liposomesP Reynier, D Briane, A Cao, et al.British Journal of Haematology|November 1, 1994
Homozygous beta-thalassaemia resulting in the beta-thalassaemia carrier state phenotypeM C Rosatelli, A Pischedda, A Meloni, et al.Journal of Immunology (Baltimore, Md. : 1950)|August 26, 1998
The invariant chain gene intronic enhancer shows homology to class II promoter elementsB B Moore, Z A Cao, T L McRae, et al.Human Mutation|January 1, 1992
A novel beta-globin structural mutant, Hb Brescia (beta 114 Leu-Pro), causing a severe beta-thalassemia intermedia phenotypeS Murru, D Poddie, G V Sciarratta, et al.American Journal of Obstetrics and Gynecology|January 1, 1993
Early transabdominal chorionic villus sampling in couples at high genetic riskG Monni, R M Ibba, R Lai, et al.Blood|December 1, 1979
Molecular basis of hemoglobin-H disease in the Mediterranean populationY W Kan, A M Dozy, G Stamatoyannopoulos, et al.Studies in Health Technology and Informatics|April 9, 2008
Eye gaze tracking for endoscopic camera positioning: an application of a hardware/software interface developed to automate AesopS M Ali, L A Reisner, B King, et al.American Journal of Medical Genetics|April 1, 1992
X-linked mental retardation and characteristic physical features in two brothers with duplication Xp22-XpterC Cianchetti, F Muntoni, A M Falchi, et al.Pageof 37