209 related articles for article (PubMed ID: 15182058)
1. Thalassemia intermedia due to co-inheritance of beta0/beta(+)-thalassemia and (- -SEA) alpha-thalassemia/Hb Westmead [alpha122(H5)His > Gln (alpha2)] in a Chinese family.
Wong WS; Chan AY; Yip SF; Ma ES
Hemoglobin; 2004 May; 28(2):151-6. PubMed ID: 15182058
[TBL] [Abstract][Full Text] [Related]
2. High-resolution melting analysis of the three common nondeletional α-thalassemia mutations in the Chinese population: Hbs Constant Spring, Quong Sze and Westmead.
Li R; Liao C; Li D; Li J
Hemoglobin; 2010; 34(6):587-93. PubMed ID: 21077768
[TBL] [Abstract][Full Text] [Related]
3. Hb Westmead (
Jiang F; Ju AP; Li J; Chen GL; Zhou JY; Tang XW; Zuo LD; Li DZ
Hemoglobin; 2020 May; 44(3):153-155. PubMed ID: 32436451
[TBL] [Abstract][Full Text] [Related]
4. Thalassemia intermedia in HbH-CS disease with compound heterozygosity for beta-thalassemia: challenges in hemoglobin analysis and clinical diagnosis.
Tan JA; Kok JL; Tan KL; Wee YC; George E
Genes Genet Syst; 2009 Feb; 84(1):67-71. PubMed ID: 19420802
[TBL] [Abstract][Full Text] [Related]
5. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
Viprakasit V; Ekwattanakit S; Chalaow N; Riolueang S; Wijit S; Tanyut P; Chat-Uthai N; Tachavanich K
Acta Haematol; 2014; 131(2):88-94. PubMed ID: 24081251
[TBL] [Abstract][Full Text] [Related]
6. Complex Interaction of Hb Q-Thailand with α
He S; Qin Q; Lin L; Chen Q; Yi S; Wei H; Du J; Zheng C; Qiu X; Chen B
Hemoglobin; 2017 Jan; 41(1):68-72. PubMed ID: 28475397
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 22239481
[TBL] [Abstract][Full Text] [Related]
8. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
Zhu BS; He J; Zhang J; Zeng XH; Su J; Xu XH; Li SY; Chen H; Zhang YH
Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
[TBL] [Abstract][Full Text] [Related]
9. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E
Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
[TBL] [Abstract][Full Text] [Related]
10. [Analysis of hematological phenotype and genotype of 23 patients from Guangdong with co-inherited hemoglobin Hb Westmead and β-thalassemia].
Yan M; Gan X; Liu M; Huang B; Zhong L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):598-601. PubMed ID: 27577202
[TBL] [Abstract][Full Text] [Related]
11. [Study on gene mutations of alpha-thalassemia in the South of China].
Duan S; Li HY; Chen Z; Chen SQ; Bi XJ; Chen LM; Du CS
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2003 Feb; 11(1):54-60. PubMed ID: 12667291
[TBL] [Abstract][Full Text] [Related]
12. Mild beta-thalassemia intermedia caused by compound heterozygosity for (G)gamma((A)gammadeltabeta)(o)/beta-thalassemia and molecular characterization of the defect in four Chinese families.
Tan Jin Ai MA; Yap SF; Tan KL; Wong YC; Wee YC; Kok JL
Acta Haematol; 2003; 109(4):169-75. PubMed ID: 12853688
[TBL] [Abstract][Full Text] [Related]
13. Hb Duan [alpha 75(EF4)Asp----Ala], Hb Westmead [alpha 122(H5)His----Gln], and alpha-thalassemia-2 (-4.2 Kb deletion) in a Chinese family.
Liang S; Tang Z; Su C; Lung Q; Liang R; Fei YJ; Kutlar F; Wilson JB; Webber BB; Hu H
Hemoglobin; 1988; 12(1):13-21. PubMed ID: 3384694
[TBL] [Abstract][Full Text] [Related]
14. The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity.
Chen W; Zhang X; Shang X; Cai R; Li L; Zhou T; Sun M; Xiong F; Xu X
BMC Med Genet; 2010 Feb; 11():31. PubMed ID: 20181291
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. beta-thalassemia intermedia caused by compound heterozygosity for Hb Malay (beta codon 19 AAC-->AGC; asn-->Ser) and codons 41/42 (-CTTT) beta(0)-thalassemia mutation.
Ma SK; Chow EY; Chan AY; Kung NN; Waye JS; Chan LC; Chui DH
Am J Hematol; 2000 Jul; 64(3):206-9. PubMed ID: 10861818
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
Moassas F; Nweder MS; Murad H
BMC Pediatr; 2019 Feb; 19(1):61. PubMed ID: 30777047
[TBL] [Abstract][Full Text] [Related]
19. Clinical phenotype of triplicated alpha-globin genes and heterozygosity for beta0-thalassemia in Chinese subjects.
Ma SK; Au WY; Chan AY; Chan LC
Int J Mol Med; 2001 Aug; 8(2):171-5. PubMed ID: 11445869
[TBL] [Abstract][Full Text] [Related]
20. [Analysis of the non-deletion alpha-thalassemia mutations by PCR temperature gradient gel electrophoresis].
Zhao Y; Xu X; Yang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):51-5. PubMed ID: 11172644
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]