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Items: 1 to 20 of 116

1.
2.

Molecular characterization of a novel 27.6-kb deletion causing α(+) thalassemia in a Chinese family.

Wei XF, Shang X, He DQ, Huang JW, Zhang XH, Xu XM.

Ann Hematol. 2011 Jan;90(1):17-22. doi: 10.1007/s00277-010-1030-1. Epub 2010 Jul 20.

PMID:
20645100
3.

A rare Hb H disease due to the - -(SEA) and 16.6 kb α-thalassemia-2 deletions.

Sroymora S, Jindadamrongwech S, Butthep P, Chuncharunee S.

Hemoglobin. 2012;36(2):200-4. doi: 10.3109/03630269.2012.655355. Epub 2012 Feb 29.

PMID:
22376301
4.

A novel fusion gene and a common α(0)-thalassemia deletion cause hemoglobin H disease in a Chinese family.

Huang JW, Shang X, Zhao Y, Cai R, Zhang XH, Wei XF, Xiong F, Xu XM.

Blood Cells Mol Dis. 2013 Jun;51(1):31-4. doi: 10.1016/j.bcmd.2013.01.013. Epub 2013 Mar 6.

PMID:
23481460
5.

Hemoglobin H disease due to a de novo mutation at the α2-globin gene and an inherited common α-thalassemia deletion found in a Chinese boy.

Zhu C, Yu W, Xie J, Chen L, Ding H, Shang X, Xu X.

Blood Cells Mol Dis. 2010 Oct 15;45(3):223-6. doi: 10.1016/j.bcmd.2010.07.005. Epub 2010 Aug 6.

PMID:
20691621
6.
7.

A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease.

Farashi S, Faramarzi Garous N, Zeinali F, Vakili S, Ashki M, Imanian H, Najmabadi H, Azarkeivan A, Tamaddoni A.

Hemoglobin. 2015;39(3):196-200. doi: 10.3109/03630269.2015.1030757. Epub 2015 May 15.

PMID:
25976776
8.

Identification of one or two α-globin gene deletions by isoelectric focusing electrophoresis.

Agarwal AM, Nussenzveig RH, Hoke C, Lorey TS, Greene DN.

Am J Clin Pathol. 2013 Sep;140(3):301-5. doi: 10.1309/AJCPF4UIJKH3EOBY.

PMID:
23955447
9.

Identification of the -α(2.4) Deletion in One Family and in One Hb H Disease Patient in Guangxi, People's Republic of China.

Pang W, Sun L, Long J, Weng X, Ye X, Wang J, Liao Y, Tang W, Fan Z, Wu S, Song C, Wei X, Zhang C.

Hemoglobin. 2016 Jun;40(3):194-7. doi: 10.3109/03630269.2016.1153486. Epub 2016 Mar 17.

PMID:
26984456
10.

Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.

Lie-Injo LE, Herrera AR, Lebo RV, Hassan K, Lopez CG.

Am J Hematol. 1985 Mar;18(3):289-96.

PMID:
2983536
11.

Novel large deletions in the human alpha-globin gene cluster: Clarifying the HS-40 long-range regulatory role in the native chromosome environment.

Coelho A, Picanço I, Seuanes F, Seixas MT, Faustino P.

Blood Cells Mol Dis. 2010 Aug 15;45(2):147-53. doi: 10.1016/j.bcmd.2010.05.010. Epub 2010 Jun 30.

PMID:
20580289
12.

Screening for common nondeletional α-thalassemias in Chinese newborns by determination of Hb Bart's using the Sebia Capillarys 2 electrophoresis system.

Tang HS, Zhou JY, Xie XM, Li R, Liao C, Li DZ.

Hemoglobin. 2012;36(2):196-9. doi: 10.3109/03630269.2011.649151. Epub 2012 Jan 12.

PMID:
22239481
13.

Novel 31.2 kb α0 Deletion in a Palestinian Family with α-Thalassemia.

Brieghel C, Birgens H, Frederiksen H, Hertz JM, Steenhof M, Petersen J.

Hemoglobin. 2015;39(5):346-9. doi: 10.3109/03630269.2015.1054512. Epub 2015 Jun 26.

PMID:
26114741
14.

A novel alpha-thalassemia-2 (-2.7-kb) observed in a Chinese patient with Hb H disease.

Zhao JB, Zhao L, Fei YJ, Liu JC, Huisman TH.

Am J Hematol. 1991 Nov;38(3):248-9.

PMID:
1951330
15.

Development of a quantitative real-time PCR assay for detection of unknown alpha-globin gene deletions.

Fallah MS, Mahdian R, Aleyasin SA, Jamali S, Hayat-Nosaeid M, Karimipour M, Raeisi M, Zeinali S.

Blood Cells Mol Dis. 2010 Jun 15;45(1):58-64. doi: 10.1016/j.bcmd.2010.03.001. Epub 2010 Apr 2.

PMID:
20363165
16.
17.

Characterization of a rare single alpha-globin gene deletion in a Chinese woman with Hb H disease.

Eng B, Walsh R, Walker L, Patterson M, Waye JS.

Hemoglobin. 2005;29(4):297-9.

PMID:
16370493
18.

The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H disease.

Orkin SH, Old J, Lazarus H, Altay C, Gurgey A, Weatherall DJ, Nathan DG.

Cell. 1979 May;17(1):33-42.

PMID:
455460
19.

The molecular basis of alpha-thalassemia in Thailand.

Winichagoon P, Fucharoen S, Wasi P.

Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:7-13.

PMID:
1298997
20.

Characterization of two unique α-globin gene cluster deletions causing α-thalassemia in Israeli Arabs.

Gilad O, Dgany O, Noy-Lotan S, Krasnov T, Elitzur S, Pissard S, Kventsel I, Yacobovich J, Tamary H.

Hemoglobin. 2014;38(5):319-24. doi: 10.3109/03630269.2014.954668. Epub 2014 Sep 15.

PMID:
25222045

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