Similar articles for PMID: 22943743

Year	Number of Results
1990	1
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1

α-thalassemia trait caused by frameshift mutations in exon 2 of the α2-globin gene: HBA2:c.131delT and HBA2:c.143delA.

Finlayson J, Ghassemifar R, Holmes P, Grey D, Newbound C, Pell N, Jennens M, Greenwood L, Beilby J. Finlayson J, et al. Hemoglobin. 2012;36(5):511-5. doi: 10.3109/03630269.2012.717053. Hemoglobin. 2012. PMID: 22943743

2

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. Waye JS, et al. Hemoglobin. 2012;36(2):205-7. doi: 10.3109/03630269.2012.656172. Epub 2012 Feb 29. Hemoglobin. 2012. PMID: 22375514

3

Hb Lynwood [α107(G14) (-T) (α2) HBA2:c.323delT)] in conjunction with the α(3.7) deletion produces a moderately severe α-thalassemia phenotype.

Finlayson J, Ghassemifar R, Holmes P, Grey D, Newbound C, Pell N, Jennens M, Macaulay C, Greenwood L, Beilby J. Finlayson J, et al. Hemoglobin. 2011;35(2):142-6. doi: 10.3109/03630269.2011.557462. Hemoglobin. 2011. PMID: 21417571

4

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. Qadah T, et al. Hemoglobin. 2012;36(3):244-52. doi: 10.3109/03630269.2012.670683. Epub 2012 Apr 23. Hemoglobin. 2012. PMID: 22524210

5

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. Joly P, et al. Hemoglobin. 2012;36(5):508-10. doi: 10.3109/03630269.2012.700898. Hemoglobin. 2012. PMID: 22738776

6

Molecular characterization of Hb Hamilton Hill (HBA2: c.388delC), a novel HBA2 variant generating a premature termination codon and truncated HBA2 chain.

Qadah T, Finlayson J, North E, Ghassemifar R. Qadah T, et al. Hemoglobin. 2015;39(2):88-94. doi: 10.3109/03630269.2015.1016958. Epub 2015 Mar 20. Hemoglobin. 2015. PMID: 25791745

7

Two novel α2 gene mutations causing altered amino acid sequences produce a mild (Hb Kinshasa, HBA2: c.428A > T) and severe (HBA2: c.342-345insCC) α-thalassemia phenotype.

Saller E, Dutly F, Frischknecht H. Saller E, et al. Hemoglobin. 2015;39(2):144-6. doi: 10.3109/03630269.2015.1008137. Epub 2015 Mar 19. Hemoglobin. 2015. PMID: 25786670

8

α(+)-Thalassemia Due to a Frameshift Mutation of the α2-Globin Gene [codons 55/56 (+T) or HBA2: c.168dup].

Waye JS, Eng B, Hanna M, Hohenadel BA, Nakamura LM, Walker L. Waye JS, et al. Hemoglobin. 2015;39(3):209-10. doi: 10.3109/03630269.2015.1030410. Epub 2015 Apr 21. Hemoglobin. 2015. PMID: 25897479

9

Nondeletional α-Thalassemia: Two New Mutations on the α2 Gene.

Ropero P, Arbeteta J, Nieto JM, González FA, González B, Villegas A, Benavente C. Ropero P, et al. Hemoglobin. 2020 Jan;44(1):17-19. doi: 10.1080/03630269.2020.1721020. Epub 2020 Jan 31. Hemoglobin. 2020. PMID: 32000548

10

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. Qadah T, et al. Hemoglobin. 2012;36(1):38-46. doi: 10.3109/03630269.2011.599086. Epub 2011 Oct 3. Hemoglobin. 2012. PMID: 21967524

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