Molecular heterogeneity of beta thalassaemia in the Italian populationGIAMPAOLO, A; MAVILIO, F; MASSA, A et al.British journal of haematology. 1984, Vol 56, Num 1, pp 79-85, issn 0007-1048Article

The prevention of thalassemia in SardiniaCAO, A; ROSATELLI, C; GALANELLO, R et al.Clinical genetics. 1989, Vol 36, Num 5, pp 277-285, issn 0009-9163, 9 p.Conference Paper

Globin synthetic ratios in homozygous β-thalassemia patients from LebanonCHEBAB, F. F; KHOURI, F. P; DEEB, S. S et al.Hemoglobin. 1984, Vol 8, Num 2, pp 151-162, issn 0363-0269Article

Successful pregnancy in β-thalassaemia majorMARTIN, K.Australian paediatric journal. 1983, Vol 19, Num 3, pp 182-183, issn 0004-993XArticle

Prescreening of beta-thalassaemia carriers: a comparison between Bayesian and other approachesSTEVE, G; ROSSI-MORI, A.Statistician (London. Print). 1983, Vol 32, Num 1-2, pp 233-239, issn 0039-0526Article

Heterozygous β-thalassemia in pregnancyCOOLEY, J. R; KITAY, D. Z.Journal of reproductive medicine. 1984, Vol 29, Num 2, pp 141-142, issn 0024-7758Article

Homozygous beta-thalassaemia in a part-aboriginal australianVOWELS, M. R; GRUNSEIT, F; WEBSTER, B. H et al.Medical journal of Australia. 1983, Vol 2, Num 3, pp 139-141, issn 0025-729XArticle

The spectrum of β-thalassaemia mutations in SicilyDI MARZO, R; DOWLING, C. E; WONG, C et al.British journal of haematology. 1988, Vol 69, Num 3, pp 393-397, issn 0007-1048Article

Towards β-globin gene-targeting with integrase-defective lentiviral vectorsDAVOUD NOURI INANLOU; YAKHCHALI, Bagher; KHANAHMAD, Hossein et al.Biotechnology letters. 2010, Vol 32, Num 11, pp 1615-1621, issn 0141-5492, 7 p.Article

Genetic modifiers of β-thalassemiaLAYTHEIN, Swee.Haematologica (Roma). 2005, Vol 90, Num 5, pp 649-660, issn 0390-6078, 12 p.Article

Plasma cyclic nucleotide levels in patients with homozygous beta-thalassaemiaPERACCHI, M; TOSCHI, V; LOMBARDI, L et al.Scandinavian journal of haematology. 1985, Vol 34, Num 4, pp 348-352, issn 0036-553XArticle

Noninvasive analysis of skin iron and zinc levels in β-thalassemia major and intermediaGORODETSKY, R; GOLDFARB, A; DAGAN, I et al.The Journal of laboratory and clinical medicine. 1985, Vol 105, Num 1, pp 44-51, issn 0022-2143Article

Hemoglobin Mississippi (β⁴⁴ser→cys): studies of the thalassemic phenotype in a mixed heterozygote with β⁺-thalassemiaSTEINBERG, M. H; ADAMS, J. G. III; MORRISON, W. T et al.The Journal of clinical investigation. 1987, Vol 79, Num 3, pp 826-832, issn 0021-9738Article

β-Thalassaemia trait in MosulKHEDER, H. H; BASHIR, F. Y.Saudi medical journal. 1990, Vol 11, Num 6, pp 460-462, issn 0379-5284, 3 p.Article

Hb Monroe or α₂β₂30(B12)Arg→Thr, a variant associated with β-thallasemia due to a G→C substitution adjacent to the donor splice site of the first intronGONZALEZ-REDONDO, J. M; STOMING, T. A; KUTLAR, F et al.Hemoglobin. 1989, Vol 13, Num 1, pp 67-74, issn 0363-0269Article

Variation in clinical severity among patients with Hb Lepore-Boston-β-thalassaemia is related to the type of β-thalassaemiaEFREMOV, D. G; EFREMOV, G. D; ZISOVSKI, N et al.British journal of haematology. 1988, Vol 68, Num 3, pp 351-355, issn 0007-1048Article

A genetic combination of silent β-thalassaemia, high Hb A₂ β-thalassaemia, and single α globin gene deletion causing mild thalassaemia intermadiaGALANELLO, R; MACCIONI, L; ROSATELLI, M. C et al.Journal of medical genetics. 1984, Vol 21, Num 2, pp 153-156, issn 0022-2593Article

Four new haplotypes observed in Algerian β-thalassemia patientsBELDJORD, C; LAPOUMEROULIE, C; BAIRD, M. L et al.Human genetics. 1983, Vol 65, Num 2, pp 204-206, issn 0340-6717Article

Iron oveload and left ventricular performance in β thalassemiaKREMASTINOS, D. T; TOUTOUZAS, P. K; VYSSOULIS, G. P et al.Acta cardiologica. 1984, Vol 39, Num 1, pp 29-40, issn 0001-5385Article

Factors affecting erythrocyte ferritin content in Thalassaemia intermediaPIPERNO, A; SAMPIETRO, M; TADDEI, M. T et al.British journal of haematology. 1984, Vol 56, Num 1, pp 173-174, issn 0007-1048Article

Fifth Cooleýs anemia symposium, New York NY on May 30-June 1, 1984BANK, A; ANDERSON, W. F; ZAINO, E. C et al.Annals of the New York Academy of Sciences. 1985, Vol 445, issn 0077-8923, 471 p.Conference Proceedings

Determination for different severity of anemia in thalassemia: concordance and discordance among sib pairsFUCHAROEN, S; PRANEE WINICHAGOON; PENSRI POOTRAKUL et al.American journal of medical genetics. 1984, Vol 19, Num 1, pp 39-44, issn 0148-7299Article

Haemoglobin E-beta-thalassaemia: a study of eight cases in northwest IndiaGHOSH, K; CHAKRABARTHY, A. K; MOHANTY, D et al.Tropical and geographical medicine. 1983, Vol 35, Num 3, pp 267-271, issn 0041-3232Article

Global and segmental left ventricular function in β-thalassemiaKREMASTINOS, D. T; TOUTOUZAS, P. K; VYSSOULIS, G. P et al.Cardiology. 1985, Vol 72, Num 3, pp 129-139, issn 0008-6312Article

Hematological phenotype of the double heterozygous state for alpha and beta thalassemiaROSATELLI, C; FALCHI, A. M; SCALAS, M. T et al.Hemoglobin. 1984, Vol 8, Num 1, pp 25-35, issn 0363-0269Article