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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

Thalassemia intermedia in two patients with Hb Lepore-β°-thalassemia (frameshift codon 8, -AA)BOZKURT, G; BAYSAL, E; GU, L.-H et al.Hemoglobin. 1994, Vol 18, Num 3, pp 247-250, issn 0363-0269Article

Interaction of heterozygous β°-thalassemia with single functional α-globulin geneGALANELLO, R; PAGLIETTI, E; MELIS, M. A et al.American journal of hematology. 1988, Vol 29, Num 2, pp 63-66, issn 0361-8609Article

Skelettveränderungen bei der Thalassämie = Modifications osseuses dans la thalassémie = Skeletal changes in thalassemiaALAIYAN, H; MITTELMEIER, H; GRAF, N et al.Zeitschrift für Orthopädie und ihre Grenzgebiete. 1988, Vol 126, Num 4, pp 437-447, issn 0044-3220Article

Avidity of radiogallium for bone in thalassemiaGRIMMOND, A. P; SPENCER, R. P.Clinical nuclear medicine. 1987, Vol 12, Num 9, pp 758-759, issn 0363-9762Article

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

The thalassemia repositoryLANCLOS, K. D; KUTLAR, A.Hemoglobin. 1986, Vol 10, Num 5, pp 533-558, issn 0363-0269Article

Electronically determined red blood cell values in a large number of healthy black adults: subpopulations with low hemoglobin and red blood cell indicesCASTRO, O. L; HADDY, T. B; RANA, S. R et al.American journal of epidemiology. 1985, Vol 121, Num 6, pp 930-936, issn 0002-9262Article

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

Aspectos moleculares de las talasemias α y β = Molecular aspects in α and β thalassemiaIBARRA, B; PEREA, F. J; HERNANDEZ-CORDOVA, A et al.Archivos de investigación medica. 1990, Vol 21, Num 4, pp 357-362, issn 0066-6769Article

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

Osmotic fragility test in heterozygotes for α and β thalassaemiaMACCIONI, L; CAO, A.Journal of medical genetics. 1985, Vol 22, Num 5, pp 374-376, issn 0022-2593Article

Two rare mutations [CD 30(G→C) and CDs 36/37 (-T)] in a Turkish Thalassemia major patient from BulgariaJANKOVIC, L; PLASESKA, D; EFREMOV, G. D et al.Hemoglobin. 1994, Vol 18, Num 4-5, pp 359-364, issn 0363-0269Article

α°- and β°-thalassemia in a Thai family: unusually mild homozygous β°-thalassemia without α-globin gene deletionYENCHITSOMANUS, P; SUMMERS, K. M.Human genetics. 1985, Vol 69, Num 4, pp 375-377, issn 0340-6717Article

Erythrokinetics and iron status in heterozygous β thalassaemia, and the effect of interaction with α thalassaemiaPIPPARD, M. J; WAINSCOAT, J. S.British journal of haematology. 1987, Vol 66, Num 1, pp 123-127, issn 0007-1048Article

Effect of isoniazid, a haem inhibitor, on globin chain synthesis in reticulocytes from non-thalassaemic and β thalassaemic subjectsCHALEVELAKIS, G; YALOURIS, A. G; LYBERATOS, C et al.Journal of clinical pathology. 1989, Vol 42, Num 9, pp 977-981, issn 0021-9746, 5 p.Article

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

Management of Cooley's anaemiaPIOMELLI, S.Baillière's clinical haematology. 1993, Vol 6, Num 1, pp 287-298, issn 0950-3536Article

Thalassémie : physiopathologieMICHEL, G.Méditerranée médicale. 1992, Num 416, pp 79-86, issn 0302-9263Article

Thalassemia in the outpatient department of the Yangon children's hospital in Myanmar: knowledge, attitudes and practice in relation to thalassemiaKHIN EI HAN; AUNG MYO HAN; THEIN THEIN MYINT et al.Southeast Asian journal of tropical medicine and public health. 1992, Vol 23, Num 2, pp 269-272, issn 0125-1562Article

δ-thalassemia caused by disruption of the site for an erythroid-specific transcription factor, GATA-1, in the δ-globin gene promoterMATSUDA, M; SAKAMOTO, N; FUKUMAKI, Y et al.Blood. 1992, Vol 80, Num 5, pp 1347-1351, issn 0006-4971Article

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

Red cell alloantibodies in patients with thalassemiaSPANOS, T; KARAGEORGA, M; LADIS, V et al.Vox sanguinis (Basel. 1956). 1990, Vol 58, Num 1, pp 50-55, issn 0042-9007Article

The interaction of alpha thalassaemia and sickle cell-beta° thalassaemiaVYAS, P; HIGGS, D. R; WEATHERALL, D. J et al.British journal of haematology. 1988, Vol 70, Num 4, pp 449-454, issn 0007-1048Article