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.
422 related articles for article (PubMed ID: 18932069)
1. Hb Lepore-Leiden: a new delta/beta rearrangement associated with a beta-thalassemia minor phenotype. Harteveld CL; Wijermans PW; Arkesteijn SG; Van Delft P; Kerkhoffs JL; Giordano PC Hemoglobin; 2008; 32(5):446-53. PubMed ID: 18932069 [TBL] [Abstract][Full Text] [Related]
2. Mutational spectrum of delta-globin gene in the Portuguese population. Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081 [TBL] [Abstract][Full Text] [Related]
3. A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with beta(0)-thalassaemia. So CC; Chan AY; Tsang ST; Lee AC; Au WY; Ma ES; Chan LC Br J Haematol; 2007 Jan; 136(1):158-62. PubMed ID: 17222202 [TBL] [Abstract][Full Text] [Related]
4. Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation. Moumni I; Zorai A; Daoued BB; Mosbahi I; Omar S; Kaabachi N; Dellagi K; Abbes S Hemoglobin; 2007; 31(1):23-9. PubMed ID: 17365002 [TBL] [Abstract][Full Text] [Related]
6. Beta-thalassemia in association with a new delta-chain hemoglobin variant [delta116(g18)Arg-->Leu]: implications for carrier screening and prenatal diagnosis. Waye JS; Patterson M; Walker L; Eng B; Nakamura LM; Lafferty JD; Yong SL; Wu JK; Chui DH Am J Hematol; 2003 Nov; 74(3):179-81. PubMed ID: 14587045 [TBL] [Abstract][Full Text] [Related]
7. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster. Esteghamat F; Imanian H; Azarkeivan A; Pourfarzad F; Almadani N; Najmabadi H Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380 [TBL] [Abstract][Full Text] [Related]
8. A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]. Moumni I; Zorai A; Mahjoub S; Mosbahi I; Chaouechi D; Benromdhane N; Abbes S Hemoglobin; 2014; 38(2):88-90. PubMed ID: 24471655 [TBL] [Abstract][Full Text] [Related]
9. Beta-, delta beta-thalassemia and Hb lepore among Yugoslav, Bulgarian, Turkish and Albanian. Efremov GD Haematologica; 1990; 75 Suppl 5():31-41. PubMed ID: 2086380 [TBL] [Abstract][Full Text] [Related]
10. Hb A2 Hong Kong - A novel δ-globin variant in a Chinese family masks the diagnosis of β-thalassemia trait. So CC; Chan AY; Luo HY; Verhovsek M; Chui DH; Ling SC; Chan LC Hemoglobin; 2011; 35(2):162-5. PubMed ID: 21417575 [TBL] [Abstract][Full Text] [Related]
11. New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG]. Phylipsen M; Harteveld CL; de Metz M; Gallivan MV; Arkesteijn SG; Luo HY; Chui DH; Giordano PC Hemoglobin; 2010; 34(5):445-50. PubMed ID: 20854118 [TBL] [Abstract][Full Text] [Related]
12. Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine). Coleman MB; Lu ZH; Smith CM; Adams JG; Harrell A; Plonczynski M; Steinberg MH J Clin Invest; 1995 Feb; 95(2):503-9. PubMed ID: 7860732 [TBL] [Abstract][Full Text] [Related]
13. Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in Cis. Colaco S; Trivedi A; Colah RB; Ghosh K; Nadkarni AH Hemoglobin; 2014; 38(1):24-7. PubMed ID: 24200152 [TBL] [Abstract][Full Text] [Related]
14. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience. Basak AN Hemoglobin; 2007; 31(2):233-41. PubMed ID: 17486506 [TBL] [Abstract][Full Text] [Related]
15. Association of beta-thalassemia and Hb Q-Thailand resulting in a normal Hb A2 value. Liao C; Li J; Li D Hemoglobin; 2008; 32(5):505-8. PubMed ID: 18932077 [TBL] [Abstract][Full Text] [Related]
16. [Detection of beta thalassemia by the technique of refractory amplification of mutation systems (ARMS-PCR)]. Bravo M; Salazar R; Arends A; Alvarez M; Velázquez D; Guevara JM; Castillo O Invest Clin; 1999 Sep; 40(3):203-13. PubMed ID: 10531753 [TBL] [Abstract][Full Text] [Related]
17. β-Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β-Thalassemia is Rare in the Indian Population. Sreedharanunni S; Chhabra S; Hira JK; Bansal D; Sharma P; Das R Hemoglobin; 2015; 39(5):362-5. PubMed ID: 26291970 [TBL] [Abstract][Full Text] [Related]
18. Spontaneous mutation of the hemoglobin Leiden (beta 6 or 7 Glu-->0) in a Thai girl. Sanguansermsri P; Shimbhu D; Wongvilairat R; Pimsorn C; Sanguansermsri T Haematologica; 2003 Dec; 88(12):ECR35. PubMed ID: 14688008 [TBL] [Abstract][Full Text] [Related]
19. Symptomatic erythrocytosis associated with a compound heterozygosity for Hb Lepore-Boston-Washington (δ87-β116) and Hb Johnstown [β109(G11)Val→Leu, GTG>TTG]. Inoue S; Oliveira JL; Hoyer JD; Sharman M Hemoglobin; 2012; 36(4):362-70. PubMed ID: 22563907 [TBL] [Abstract][Full Text] [Related]
20. The molecular basis of normal HbA2 (type 2) beta-thalassemia in Greece. Tzetis M; Traeger-Synodinos J; Kanavakis E; Metaxotou-Mavromati A; Kattamis C Hematol Pathol; 1994; 8(1-2):25-34. PubMed ID: 8034555 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]