190 related articles for article (PubMed ID: 19420802)
21. Alpha-thalassaemia in association with beta-thalassaemia patients in Malaysia: a study on the co-inheritance of both disorders.
Wee YC; Tan KL; Kuldip K; Tai KS; George E; Tan PC; Chia P; Subramaniam R; Yap SF; Tan JA
Community Genet; 2008; 11(3):129-34. PubMed ID: 18376108
[TBL] [Abstract][Full Text] [Related]
22. Analysis of rare thalassemia caused by HS-40 regulatory site deletion.
Luo S; Chen X; Zhong Q; Wang Q; Xu Z; Qin L; Wang J; Yuan D; Yan T; Tang N
Hematology; 2020 Dec; 25(1):286-291. PubMed ID: 32720864
[No Abstract] [Full Text] [Related]
23. Hematological characterization of compound heterozygous hemoglobin Hope/E patients with and without alpha-thalassemia-1 SEA type deletion.
Pornprasert S
Clin Lab; 2013; 59(9-10):1183-5. PubMed ID: 24273946
[TBL] [Abstract][Full Text] [Related]
24. A novel α(0) -thalassemia deletion in a Greek patient with HbH disease and β-thalassemia trait.
Phylipsen M; Traeger-Synodinos J; van der Kraan M; van Delft P; Bakker G; Geerts M; Kanavakis E; Stamoulakatou A; Karagiorga M; Giordano PC; Harteveld CL
Eur J Haematol; 2012 Apr; 88(4):356-62. PubMed ID: 22324317
[TBL] [Abstract][Full Text] [Related]
25. α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (
Panyasai S; Phasit A
Hemoglobin; 2020 Jul; 44(4):264-271. PubMed ID: 32727229
[TBL] [Abstract][Full Text] [Related]
26. Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β
Li Y; Yan JM; Zhou JY; Lu YC; Li DZ
Hemoglobin; 2017 Jan; 41(1):47-49. PubMed ID: 28366026
[TBL] [Abstract][Full Text] [Related]
27. Haemoglobinopathies in southeast Asia.
Fucharoen S; Winichagoon P
Indian J Med Res; 2011 Oct; 134(4):498-506. PubMed ID: 22089614
[TBL] [Abstract][Full Text] [Related]
28. [A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].
Li Q; Li LY; Mo QH
Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jan; 28(1):16-9. PubMed ID: 18227017
[TBL] [Abstract][Full Text] [Related]
29. [Application of Next Generation Sequencing to Screen the Neonatal Thalassemia Genes].
Tan M; Lu S; Wu LS; Jin DW; Peng ZY; Chen Y
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2015 Oct; 23(5):1404-9. PubMed ID: 26524047
[TBL] [Abstract][Full Text] [Related]
30. Hb Athens-Georgia (beta 40(C6) Arg > Lys, HBB:c.122G > A) with a single α-globin gene (Hb H disease) in a Thai family: molecular, hematological, and diagnostic aspects.
Panyasai S; Kunyanone N; Satthakarn S
Scand J Clin Lab Invest; 2021 Feb; 81(1):52-58. PubMed ID: 33287582
[TBL] [Abstract][Full Text] [Related]
31. Hb A2/E levels found in co-inheritance with the α-thalassemia-1 - -(SEA)/type deletion and either Hb E or β-thalassemia.
Pornprasert S; Treesuwan K; Punyamung M; Kongthai K
Hemoglobin; 2012; 36(4):381-7. PubMed ID: 22563848
[TBL] [Abstract][Full Text] [Related]
32. Transfusion-dependent thalassemia in Northern Sarawak: a molecular study to identify different genotypes in the multi-ethnic groups and the importance of genomic sequencing in unstudied populations.
Tan JA; Chin SS; Ong GB; Mohamed Unni MN; Soosay AE; Gudum HR; Kho SL; Chua KH; Chen JJ; George E
Public Health Genomics; 2015; 18(1):60-4. PubMed ID: 25412720
[TBL] [Abstract][Full Text] [Related]
33. [Hb Bart's Quantitative Analysis in the Screening of α-Thalassemia].
Yi S; Wang B; Li H; Zhang H; Song JP
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2021 Dec; 29(6):1903-1906. PubMed ID: 34893131
[TBL] [Abstract][Full Text] [Related]
34. [Analysis of the Types of Thalassemia Gene Mutations in Nanping Area of Fujian, China].
Chen MF; Huang MZ; Lin Q; Huang J; Chen F; Zhang JY; Xue F
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2020 Jun; 28(3):918-926. PubMed ID: 32552958
[TBL] [Abstract][Full Text] [Related]
35. Co-inheritance of alpha-and beta-thalassemia in Khuzestan Province, Iran.
Rahim F; Kaikhaei B; Zandian K; Hoseini A
Hematology; 2008 Feb; 13(1):59-64. PubMed ID: 18534068
[TBL] [Abstract][Full Text] [Related]
36. Interaction of Hb South Florida (codon 1; GTG-->ATG) and HbE, with beta-thalassemia (IVS1-1; G-->A): expression of different clinical phenotypes.
Tan JA; Tan KL; Omar KZ; Chan LL; Wee YC; George E
Eur J Pediatr; 2009 Sep; 168(9):1049-54. PubMed ID: 19034506
[TBL] [Abstract][Full Text] [Related]
37. Compound Heterozygosity for an Unstable Novel Hemoglobin Variant, Hb Dongguan [α52(E1)Ser→Cys (T
Chen WD; Ren YX; Wang YJ; Xie WJ; Li J; Xu AP; Ji L
Hemoglobin; 2019; 43(4-5):286-288. PubMed ID: 31650882
[TBL] [Abstract][Full Text] [Related]
38. Co-inherited β-thalassemia trait and HbH disease: clinical characteristics and interference in diagnosis of thalassemia by high-performance liquid chromatography.
Yin XL; Wu ZK; Zhou XY; Zhou TH; Zhou YL; Wang L; Huang J; Zhang XH
Int J Lab Hematol; 2012 Aug; 34(4):427-31. PubMed ID: 22433173
[TBL] [Abstract][Full Text] [Related]
39. Molecular analysis of alpha- and beta-thalassemia in Meizhou region and comparison of gene mutation spectrum with different regions of southern China.
Wu H; Huang Q; Yu Z; Zhong Z
J Clin Lab Anal; 2021 Dec; 35(12):e24105. PubMed ID: 34752669
[TBL] [Abstract][Full Text] [Related]
40. Screening for co-existence of α-thalassemia in β-thalassemia and in HbE heterozygotes via an enzyme-linked immunosorbent assay for Hb Bart's and embryonic ζ-globin chain.
Tatu T; Kiewkarnkha T; Khuntarak S; Khamrin S; Suwannasin S; Kasinrerk W
Int J Hematol; 2012 Apr; 95(4):386-93. PubMed ID: 22438184
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
