HbH disease associated with the (-^MED) deletion in a Brazilian black womanSONATI, M. F; KIMURA, E. M; GROTTO, H. Z. W et al.Acta haematologica. 1992, Vol 87, Num 3, pp 145-147, issn 0001-5792Article

β-Thalassemia intermedia and IVS-1 NT6 homozygosis in BrazilCOSTA, F. F; TAVELLA, M. H; ZAGO, M. A et al.Brazilian journal of medical and biological research. 1991, Vol 24, Num 2, pp 157-161, issn 0100-879X, 5 p.Article

Factor XIII Val34Leu is a genetic factor involved in the aetiology of venous thrombosisFRANCO, R. F; REITSMA, P. H; LOURENCO, D et al.Thrombosis and haemostasis. 1999, Vol 81, Num 5, pp 676-679, issn 0340-6245Article

Interpopulational and intrapopulational genetic diversity of Amerindians as revealed by six variable number of tandem repeatsZAGO, M. A; SILVA, W. A; TAVELLA, M. H et al.Human heredity. 1996, Vol 46, Num 5, pp 274-289, issn 0001-5652Article

Are haemochromatosis mutations related to the severity of liver disease in hepatitis C virus infection?MARTINELLI, A. L. C; FRANCO, R. F; VILLANOVA, M. G et al.Acta haematologica. 1999, Vol 102, Num 3, pp 152-156, issn 0001-5792Article

Heterogeneous ethnic distribution of the 844ins68 in the cystathionine β-synthase geneFRANCO, R. F; ELION, J; LAVINHA, J et al.Human heredity. 1998, Vol 48, Num 6, pp 338-342, issn 0001-5652Article

Atypical β^S haplotypes are generated by diverse genetic mechanismsZAGO, M. A; SILVA, W. A; KRISHNAMOORTHY, R et al.American journal of hematology. 2000, Vol 63, Num 2, pp 79-84, issn 0361-8609Article

Factor XIII Val34Leu and the risk of myocardial infarctionFRANCO, R. F; PAZIN-FILHO, A; TAVELLA, M. H et al.Haematologica (Roma). 2000, Vol 85, Num 1, pp 67-71, issn 0390-6078Article

A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic diseaseFRANCO, R. F; MORELLI, V; LOURENCO, D et al.British journal of haematology. 1999, Vol 105, Num 2, pp 556-559, issn 0007-1048Article

Prevalence of the G20210A polymorphism in the 3'-untranslated region of the prothrombin gene in different human populationsFRANCO, R. F; SANTOS, S. E. B; ELION, J et al.Acta haematologica. 1998, Vol 100, Num 1, pp 9-12, issn 0001-5792Article

Factor V Arg³⁰⁶→ Thr (factor V Cambridge) and factor V Arg³⁰⁶→ Gly mutations in venous thrombotic diseaseFRANCO, R. F; MAFFEI, F. H; LOURENCO, D et al.British journal of haematology. 1998, Vol 103, Num 3, pp 888-890, issn 0007-1048Article

Racial heterogeneity of DNA polymorphisms linked to the A and the O alleles of the ABO blood group geneZAGO, M. A; TAVELLA, M. H; SIMOES, B. P et al.Annals of human genetics. 1996, Vol 60, pp 67-72, issn 0003-4800, 1Article