151 related articles for article (PubMed ID: 16343256)
1. 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]
2. 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]
3. 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]
4. [Genetic screening for alpha-thalassemia deletional determinants by GapPCR method].
Katol J; Takao M; Ideguchi H; Sawada H; Kawashima H; Ono J
Rinsho Byori; 2006 Nov; 54(11):1095-100. PubMed ID: 17240829
[TBL] [Abstract][Full Text] [Related]
5. Prevalence of α-thalassaemia genotypes in pregnant women in northern Thailand.
Pharephan S; Sirivatanapa P; Makonkawkeyoon S; Tuntiwechapikul W; Makonkawkeyoon L
Indian J Med Res; 2016 Mar; 143(3):315-22. PubMed ID: 27241645
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Molecular characterization of α- and β-thalassaemia among Malay patients.
Yatim NF; Rahim MA; Menon K; Al-Hassan FM; Ahmad R; Manocha AB; Saleem M; Yahaya BH
Int J Mol Sci; 2014 May; 15(5):8835-45. PubMed ID: 24857915
[TBL] [Abstract][Full Text] [Related]
8. High prevalence of alpha-thalassemia among individuals with microcytosis and hypochromia without anemia.
Borges E; Wenning MR; Kimura EM; Gervásio SA; Costa FF; Sonati MF
Braz J Med Biol Res; 2001 Jun; 34(6):759-62. PubMed ID: 11378664
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. alpha-globin genes: thalassemic and structural alterations in a Brazilian population.
Wenning MR; Kimura EM; Costa FF; Saad ST; Gervásio S; de Jorge SB; Borges E; Silva NM; Sonati MF
Braz J Med Biol Res; 2000 Sep; 33(9):1041-5. PubMed ID: 10973135
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Detection of maternal carriers of common α-thalassemia deletions from cell-free DNA.
Doan PL; Nguyen DA; Le QT; Hoang DT; Nguyen HD; Nguyen CC; Doan KPT; Tran NT; Ha TMT; Trinh THN; Nguyen VT; Bui CT; Lai NT; Duong TH; Mai HL; Huynh PV; Huynh TTT; Le QV; Vo TB; Dao TH; Vo PA; Le DN; Tran NNT; Tran QNT; Van YT; Tran HT; Nguyen HT; Nguyen PU; Do TT; Truong DK; Tang HS; Cao NT; Lam TT; Tran LS; Nguyen HN; Giang H; Phan MD
Sci Rep; 2022 Aug; 12(1):13581. PubMed ID: 35945425
[TBL] [Abstract][Full Text] [Related]
13. Molecular defects in the beta-globin gene identified in different ethnic groups/populations during prenatal diagnosis for beta-thalassemia: a Malaysian experience.
Tan JA; George E; Tan KL; Chow T; Tan PC; Hassan J; Chia P; Subramanium R; Chandran R; Yap SF
Clin Exp Med; 2004 Dec; 4(3):142-7. PubMed ID: 15599663
[TBL] [Abstract][Full Text] [Related]
14. Detection of common deletional alpha-thalassemia spectrum by molecular technique in kelantan, northeastern malaysia.
Rosnah B; Rosline H; Zaidah AW; Noor Haslina MN; Marini R; Shafini MY; Nurul Ain FA
ISRN Hematol; 2012; 2012():462969. PubMed ID: 22888447
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Genetic Diagnosis of Thalassemia in Baise, Guangxi Zhuang Autonomous Region].
Lu H; Qin Q; Li JH; Chen T; Liang SJ; Lu XS
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2021 Jun; 29(3):865-868. PubMed ID: 34105485
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [Analysis of genotype and hematological phenotype of 14 patients with coinheritance HKαα and South-East deletion thalassemia].
Zhong LY; Wang F; Chen PS; Xie YJ; Tan JY; Liu M; Huang B; Lin WB
Zhonghua Yi Xue Za Zhi; 2018 Jan; 98(2):117-121. PubMed ID: 29343036
[No Abstract] [Full Text] [Related]
19. Identification of a novel 91.5 kb-deletion (αα)
Xu L; Chen M; Zheng J; Zhang S; Zhang M; Chen L; He Q; Guo D; Lin N; Huang H
J Matern Fetal Neonatal Med; 2023 Dec; 36(2):2254890. PubMed ID: 37673790
[TBL] [Abstract][Full Text] [Related]
20. Genetic research and clinical analysis of deletional Chinese
Wu Y; Yao Q; Zhong M; Wu J; Xie L; Su L; Yu F
Ann Hematol; 2020 Dec; 99(12):2747-2753. PubMed ID: 32930850
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
