190 related articles for article (PubMed ID: 19420802)
1. 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]
2. 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]
3. [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]
4. 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]
5. Heterogeneity in alpha-thalassemia interactions in Malays, Chinese and Indians in Malaysia.
Wee YC; Tan KL; Chow TW; Yap SF; Tan JA
J Obstet Gynaecol Res; 2005 Dec; 31(6):540-6. PubMed ID: 16343256
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. [Gene Mutation Types of Thalassemia in Chongzuo Childbearing-age Population of Guangxi Zhuang Autonomous Region of China].
Li DM; Huang XN; Zhao H; Chen X; Yang WW; Peng ZR; Liang LF; Chen BY; He S
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2023 Dec; 31(6):1804-1810. PubMed ID: 38071064
[TBL] [Abstract][Full Text] [Related]
8. Molecular characteristic of alpha thalassaemia among patients diagnosed in UKM Medical Centre.
Azma RZ; Ainoon O; Hafiza A; Azlin I; Noor Farisah AR; Nor Hidayati S; Noor Hamidah H
Malays J Pathol; 2014 Apr; 36(1):27-32. PubMed ID: 24763232
[TBL] [Abstract][Full Text] [Related]
9. DNA studies are necessary for accurate patient diagnosis in compound heterozygosity for Hb Adana (HBA2:c.179>A) with deletional or nondeletional α-thalassaemia.
Tan JAMA; Kho SL; Ngim CF; Chua KH; Goh AS; Yeoh SL; George E
Sci Rep; 2016 Jun; 6():26994. PubMed ID: 27271331
[TBL] [Abstract][Full Text] [Related]
10. [Methodological study for detecting gene mutation of family with genotyping of compound heterogenicity of SEA alpha-thalassemia 1 and HbCS].
Chen J; Luo B; Qi Z; Huo PD; Zhang QS; Wang H
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Jun; 18(3):675-8. PubMed ID: 20561426
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Prenatal diagnosis of a rare β-thalassemia gene -90 (C>T) (HBB: c.-140 C>T) mutation associated with deletional Hb H disease (--
Qian H; Huang J; Xu J; Zhao W; Ye X; Liu W
Mol Genet Genomic Med; 2020 Nov; 8(11):e1472. PubMed ID: 32885601
[TBL] [Abstract][Full Text] [Related]
13. Application of an expanded multiplex genotyping assay for the simultaneous detection of Hemoglobin Constant Spring and common deletional alpha-thalassemia mutations.
Kidd JL; Azimi M; Lubin B; Vichinsky E; Hoppe C
Int J Lab Hematol; 2010 Aug; 32(4):373-80. PubMed ID: 19919622
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Detection of Hb Constant Spring [α142, Term→Gln, TAA>CAA (α2)] in heterozygotes combined with β-thalassemia.
Li YQ; Li R; Li DZ
Hemoglobin; 2013; 37(2):197-200. PubMed ID: 23390935
[TBL] [Abstract][Full Text] [Related]
16. Hb H Hydrops Fetalis Syndrome Caused by Association of the - -(SEA) Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family.
He S; Zheng C; Meng D; Chen R; Zhang Q; Tian X; Chen S
Hemoglobin; 2015; 39(3):216-9. PubMed ID: 25897478
[TBL] [Abstract][Full Text] [Related]
17. First Case of a Compound Heterozygosity for Two Nondeletional α-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze.
Zhou JY; Yan JM; Li J; Li DZ
Hemoglobin; 2016 Jun; 40(3):210-2. PubMed ID: 26956449
[TBL] [Abstract][Full Text] [Related]
18. Genotypes of thalassemia in children: an analysis of 30 417 cases.
Li DM; He S
Zhongguo Dang Dai Er Ke Za Zhi; 2021 Aug; 23(8):841-847. PubMed ID: 34511175
[TBL] [Abstract][Full Text] [Related]
19. A case series of α-thalassemia intermedia due to compound heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] with other α-thalassemias in Malay families.
Alauddin H; Jaapar NA; Azma RZ; Ithnin A; Razak NF; Loh CK; Alias H; Abdul-Latiff Z; Othman A
Hemoglobin; 2014; 38(4):277-81. PubMed ID: 24829075
[TBL] [Abstract][Full Text] [Related]
20. Severe α-thalassemia intermedia due to a compound heterozygosity for the highly unstable Hb Adana (HBA2: c.179G>A) and a novel codon 24 (HBA2: c.75T>A) mutation.
Megawati D; Nainggolan IM; Swastika M; Susanah S; Mose JC; Harahap AR; Setianingsih I
Hemoglobin; 2014; 38(2):149-51. PubMed ID: 24351118
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]