104 related articles for article (PubMed ID: 19958200)
1. alpha-Thalassemia caused by two novel splice mutations of the alpha2-globin gene: IVS-I-1 (G>A and G>T).
Waye JS; Eng B; Dutly F; Frischknecht H
Hemoglobin; 2009; 33(6):519-22. PubMed ID: 19958200
[TBL] [Abstract][Full Text] [Related]
2. Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG).
Eng B; Walker L; Waye JS
Hemoglobin; 2009; 33(1):72-4. PubMed ID: 19205977
[TBL] [Abstract][Full Text] [Related]
3. In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (α2)].
Qadah T; Finlayson J; Ghassemifar R
Hemoglobin; 2012; 36(1):38-46. PubMed ID: 21967524
[TBL] [Abstract][Full Text] [Related]
4. alpha-Thalassemia mutation analyses in Mazandaran province, North Iran.
Tamaddoni A; Hadavi V; Nejad NH; Khosh-Ain A; Siami R; Aghai-Meibodi J; Almadani N; Oberkanins C; Law HY; Najmabadi H
Hemoglobin; 2009; 33(2):115-23. PubMed ID: 19373587
[TBL] [Abstract][Full Text] [Related]
5. Alpha-thalassemia mutations in Gilan Province, North Iran.
Hadavi V; Jafroodi M; Hafezi-Nejad N; Moghadam SD; Eskandari F; Tarashohi S; Pourfahim H; Oberkanins C; Law HY; Najmabadi H
Hemoglobin; 2009; 33(3):235-41. PubMed ID: 19657838
[TBL] [Abstract][Full Text] [Related]
6. Alpha-thalassemia phenotype induced by the new IVS-II-2 (T --> A) splice donor site mutation on the alpha2-globin gene.
Harteveld CL; Jebbink MC; van der Lely N; van Delft P; Akkermans N; Arkesteyn S; Giordano PC
Hemoglobin; 2006; 30(1):3-7. PubMed ID: 16540408
[TBL] [Abstract][Full Text] [Related]
7. Spectrum of α-globin gene mutations in the Kerman Province of Iran.
Saleh-Gohari N; Khosravi-Mashizi A
Hemoglobin; 2010; 34(5):451-60. PubMed ID: 20854119
[TBL] [Abstract][Full Text] [Related]
8. Simultaneous detection of Hb constant spring (α142, TAA>CAA, α2) and the α2 IVS-I donor site (-TGAGG) deletion by a simple polymerase chain reaction-based method in Iran.
Akhavan-Niaki H; Banihashemi A; Mostafazadeh A; Kholghi Oskooei V; Azizi M; Youssefi Kamangar R; Elmi MM
Hemoglobin; 2012; 36(2):124-30. PubMed ID: 22356652
[TBL] [Abstract][Full Text] [Related]
9. α(+)-Thalassemia trait caused by a frameshift mutation in exon 2 of the α2-globin gene [HBA2 c.244delT].
Waye JS; Walker L; Eng B
Hemoglobin; 2012; 36(2):205-7. PubMed ID: 22375514
[TBL] [Abstract][Full Text] [Related]
10. Novel mutations responsible for α-thalassemia in Iranian families.
Bayat N; Farashi S; Hafezi-Nejad N; Faramarzi N; Ashki M; Vakili S; Imanian H; Khosravi M; Azar-Keivan A; Najmabadi H
Hemoglobin; 2013; 37(2):148-59. PubMed ID: 23402770
[TBL] [Abstract][Full Text] [Related]
11. A new Frameshift mutation on the α2-globin gene causing α⁺-thalassemia: codon 43 (TTC>-TC or TTC>T-C).
Joly P; Lacan P; Garcia C; Barro C; Francina A
Hemoglobin; 2012; 36(5):508-10. PubMed ID: 22738776
[TBL] [Abstract][Full Text] [Related]
12. Molecular and cellular characterization of a new α-thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon.
Qadah T; Finlayson J; Newbound C; Pell N; Pascoe M; Greenwood L; Holmes P; Grey D; Beilby J; Ghassemifar R
Hemoglobin; 2012; 36(3):244-52. PubMed ID: 22524210
[TBL] [Abstract][Full Text] [Related]
13. A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2).
Martin G; Villegas A; González FA; Ropero P; Hojas R; Polo M; Mateo M; Salvador M; Benavente C
Hemoglobin; 2005; 29(2):113-7. PubMed ID: 15921163
[TBL] [Abstract][Full Text] [Related]
14. alpha-thalassaemia masked by beta gene defects and a new polyadenylation site mutation on the alpha2-globin gene.
Harteveld CL; Oosterhuis WP; Schoenmakers CH; Ananta H; Kos S; Bakker Verweij M; van Delft P; Arkesteijn SG; Phylipsen M; Giordano PC
Eur J Haematol; 2010 Apr; 84(4):354-8. PubMed ID: 19912309
[TBL] [Abstract][Full Text] [Related]
15. Quantification analysis of human alpha-globin gene. Mutation in 5'-splice junction sequence and alpha-thalassemia.
Iida Y
Nucleic Acids Symp Ser; 1990; (22):37-8. PubMed ID: 2101909
[TBL] [Abstract][Full Text] [Related]
16. Polymerase chain reaction-based search for two alpha-globin gene mutations in India.
Bhattacharya G; Sarkar AA; Banerjee D; Chandra S; Das M; Dasgupta UB
Hemoglobin; 2008; 32(5):485-90. PubMed ID: 18932074
[TBL] [Abstract][Full Text] [Related]
17. Frameshift mutation in the alpha2-globin gene causing alpha+ -thalassemia: codon 49 (-GC).
Eng B; Waye JS
Hemoglobin; 2008; 32(3):315-7. PubMed ID: 18473249
[TBL] [Abstract][Full Text] [Related]
18. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].
Indrák K; Divoký V; Brabec V; Indráková J; Svobodová M; Huisman TH
Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425
[TBL] [Abstract][Full Text] [Related]
19. alpha-thalassemia mutations in Khuzestan Province, Southwest Iran.
Zandian K; Nateghi J; Keikhaie B; Pedram M; Hafezi-Nejad N; Hadavi V; Oberkanins C; Azarkeivan A; Law HY; Najmabadi H
Hemoglobin; 2008; 32(6):546-52. PubMed ID: 19065332
[TBL] [Abstract][Full Text] [Related]
20. Mutations on the α2-Globin Gene That May Trigger α(+)-Thalassemia.
Farashi S; Vakili S; Garous NF; Ashki M; Imanian H; Azarkeivan A; Najmabadi H
Hemoglobin; 2015; 39(6):398-402. PubMed ID: 26329872
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
