These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Hb H disease in a Turkish family resulting from the interaction of a deletional alpha-thalassaemia-1 and a newly discovered poly A mutation. Yüregir GT; Aksoy K; Cürük MA; Dikmen N; Fei YJ; Baysal E; Huisman TH Br J Haematol; 1992 Apr; 80(4):527-32. PubMed ID: 1581238 [TBL] [Abstract][Full Text] [Related]
4. The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia. Oner R; Agarwal S; Dimovski AJ; Efremov GD; Petkov GH; Altay C; Gurgey A; Huisman TH Hemoglobin; 1991; 15(1-2):67-76. PubMed ID: 1717406 [TBL] [Abstract][Full Text] [Related]
5. Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene. Losekoot M; Fodde R; Harteveld CL; van Heeren H; Giordano PC; Went LN; Bernini LF J Med Genet; 1991 Apr; 28(4):252-5. PubMed ID: 1856830 [TBL] [Abstract][Full Text] [Related]
6. A new mutation in the beta-globin gene (IVS II-850 G-C) found in a Yugoslavian beta-thalassemia heterozygote. Jankovic L; Dimovski AJ; Sukarova E; Juricic D; Efremov GD Haematologica; 1992; 77(2):119-21. PubMed ID: 1398296 [TBL] [Abstract][Full Text] [Related]
8. Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene. Moi P; Loudianos G; Lavinha J; Murru S; Cossu P; Casu R; Oggiano L; Longinotti M; Cao A; Pirastu M Blood; 1992 Jan; 79(2):512-6. PubMed ID: 1309671 [TBL] [Abstract][Full Text] [Related]
9. Hb S(C)-beta+-thalassaemia: different mutations are associated with different levels of normal Hb A. Gonzalez-Redondo JM; Kutlar F; Kutlar A; Stoming TA; de Pablos JM; Kilinç Y; Huisman TH Br J Haematol; 1988 Sep; 70(1):85-9. PubMed ID: 2460127 [TBL] [Abstract][Full Text] [Related]
10. Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations. Murru S; Loudianos G; Deiana M; Camaschella C; Sciarratta GV; Agosti S; Parodi MI; Cerruti P; Cao A; Pirastu M Blood; 1991 Mar; 77(6):1342-7. PubMed ID: 2001456 [TBL] [Abstract][Full Text] [Related]
11. Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia. Divoky V; Bissé E; Wilson JB; Gu LH; Wieland H; Heinrichs I; Prior JF; Huisman TH Biochim Biophys Acta; 1992 Dec; 1180(2):173-9. PubMed ID: 1463768 [TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia major. Yang KG; Kutlar F; George E; Wilson JB; Kutlar A; Stoming TA; Gonzalez-Redondo JM; Huisman TH Br J Haematol; 1989 May; 72(1):73-80. PubMed ID: 2736244 [TBL] [Abstract][Full Text] [Related]
18. Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene. Cai SP; Eng B; Francombe WH; Olivieri NF; Kendall AG; Waye JS; Chui DH Blood; 1992 Mar; 79(5):1342-6. PubMed ID: 1536956 [TBL] [Abstract][Full Text] [Related]
20. Thalassemia due to a mutation in the cleavage-polyadenylation signal of the human beta-globin gene. Orkin SH; Cheng TC; Antonarakis SE; Kazazian HH EMBO J; 1985 Feb; 4(2):453-6. PubMed ID: 4018033 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]