Hb S(C)-β⁺-thalassaemia: different mutations are associated with different levels of normal Hb AGONZALEZ-REDONDO, J. M; KUTLAR, F; KUTLAR, A et al.British journal of haematology. 1988, Vol 70, Num 1, pp 85-89, issn 0007-1048Article

Pitfalls in genetic counselling for β-thalassemia: an individual with 4 different thalassemia mutationsGALANELLO, R; PAGLIETTI, M. E; ADDIS, M et al.Clinical genetics. 1988, Vol 33, Num 3, pp 151-155, issn 0009-9163Article

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

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

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

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

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

Haematological phenotypes in a family with triplicated α-globin gene, β°₃₉ and δ⁺₂₇ thalassaemia mutationsOGGIANO, L; RIMINI, E; FROGHERI, L et al.Clinical and laboratory haematology. 1992, Vol 14, Num 4, pp 289-292, issn 0141-9854Article

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

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

Association of heterocellular HPFH, β⁺-thalassaemia, and δβ°-thalassaemia: haematological and molecular aspectsCIANETTI, L; CARE, A; SASSO, G. F et al.Journal of medical genetics. 1984, Vol 21, Num 4, pp 263-267, issn 0022-2593Article

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

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

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

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

Bone marrow hyperplasia of the maxillary sinuses in β-thalassemiaANDREOU, J; GOULIAMOS, A; KALOVIDOURIS, A et al.Journal of computer assisted tomography. 1984, Vol 8, Num 1, issn 0363-8715, 180Article

Dutch β⁰-thalassaemia: a 10 kilobase DNA deletion associated with significant γ-chain productionGILMAN, J. G; HUISMAN, T. H. J; ABELS, J et al.British journal of haematology. 1984, Vol 56, Num 2, pp 339-348, issn 0007-1048Article

Serum ferritin in β-thalassaemia intermediaBUONANNO, G; VALENTE, A; GONNELLA, F et al.Scandinavian journal of haematology. 1984, Vol 32, Num 1, pp 83-87, issn 0036-553XArticle

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

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