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

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

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

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

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

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

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

Succès de la thérapie génique contre la β-thalassémieDOUHI, Safi.Biofutur (Puteaux). 2010, Num 315, issn 0294-3506, p. 12Article

Quantitation of β-thalassemia genes in Quebec immigrants of Mediterranean, Southeast Asian, and Asian Indian originsKAPLAN, F; KOKOTSIS, G; CAPUA, A et al.Clinical and investigative medicine. 1991, Vol 14, Num 4, pp 325-330, issn 0147-958XArticle

Fetal hemoglobin in normal adults and β-thalassemia heterozygotesKUTLAR, A; KUTLAR, F; LI-GHAO GU et al.Human genetics. 1990, Vol 85, Num 1, pp 106-110, issn 0340-6717, 5 p.Article

Ocular abnormalities in patients with β thalassemiaGARTAGANIS, S; ISMIRIDIS, K; PAPAGEORGIOU, O et al.American journal of ophthalmology. 1989, Vol 108, Num 6, pp 699-703, issn 0002-9394Article

HB Chapel Hill or α₂74(EF3)Asp→Glyβ₂ observed in a chinese family in association with β-thalassemiaLIANG HSU; LUNG QUI-FAN; TANG ZHINING et al.Hemoglobin. 1986, Vol 10, Num 1, pp 77-86, issn 0363-0269Article

In vivo platelet activation in β-thalassemia major reflected by increased platelet-thromboxane urinary metabolitesELDOR, A; LELLOUCHE, F; GOLDFARB, A et al.Blood. 1991, Vol 77, Num 8, pp 1749-1753, issn 0006-4971Article

Mediterranean types of β-thalassemia in the German populationsLAIG, M; PAPE, M; HUNDRIESER, J et al.Human genetics. 1990, Vol 85, Num 1, pp 135-137, issn 0340-6717, 3 p.Article

Characterization of a spontaneous mutation in β-thalassemia associated with advanced paternal ageCHEHAB, F. F; WINTERHALTER, K. H; KAN, Y. W et al.Blood. 1989, Vol 74, Num 2, pp 852-854, issn 0006-4971Article

Inhibition by β-thalassemic erythrocytes of erythropoiesis in vitroVEDOVATO, M; SALVATORELLI, G.Cytobios. 1989, Vol 58, Num 232, pp 35-37, issn 0011-4529, 3 p.Article

The 12.6 kilobase DNA deletion in Dutch β°-thalassaemiaGILMAN, J. G.British journal of haematology. 1987, Vol 67, Num 3, pp 369-372, issn 0007-1048Article

Non-random association of the polymorphic Taq I restriction site, located 3KB5' to the human δ-globin gene, with the polymorphic hind III sites within the Gγ- and Aγ-globin genesPONCET, D; SALOMÉ, N; KOHEN, G et al.Acta haematologica. 1984, Vol 72, Num 4, pp 217-220, issn 0001-5792Article

Homozygous β-thalassemia without anemiaSAFAYA, S; RIEDER, R. F; DOWLING, C. E et al.Blood. 1989, Vol 73, Num 1, pp 324-328, issn 0006-4971Article

Different severity of homozygous β-thalassemia among siblingsWINICHAGOON, P; FUCHAROEN, S; THONGLAIROAM, V et al.Human genetics. 1987, Vol 76, Num 3, pp 296-297, issn 0340-6717Article

Mécanisme moléculaire des π-thalassémies = Molecular mechanism of β-thalassemiasHIRTZ, P.Lyon pharmaceutique. 1987, Vol 38, Num 3, pp 111-116, issn 0024-7804Article