124 related articles for article (PubMed ID: 21468611)
21. Hb Hubei [α114(GH2)Pro→His, HBA1: c.344C>A]: A Novel Hemoglobin Variant of the α1-Globin Chain.
Xu AP; Li J; Chen WD; Zhou Y; Ji L
Hemoglobin; 2018 May; 42(3):206-208. PubMed ID: 30277418
[TBL] [Abstract][Full Text] [Related]
22. Distribution characteristics and clinical phenotype analyses of hemoglobin variants in the Z region of Central Guangxi, Southern China.
Chen L; Tang N; Huang J; Wei X; Zhong Q; Yan T; Luo S
Hematology; 2023 Dec; 28(1):2188651. PubMed ID: 36995301
[TBL] [Abstract][Full Text] [Related]
23. Novel interactions of two α-Hb variants with SEA deletion α
Srivorakun H; Singha K; Fucharoen G; Fucharoen S
Hematology; 2018 Apr; 23(3):187-191. PubMed ID: 28945175
[TBL] [Abstract][Full Text] [Related]
24. Interaction of hemoglobin Grey Lynn (Vientiane) with a non-deletional α(+)-thalassemia in an adult Thai proband.
Singha K; Fucharoen G; Fucharoen S
Biochem Med (Zagreb); 2014; 24(1):167-74. PubMed ID: 24627726
[TBL] [Abstract][Full Text] [Related]
25. Hb Sichuan [α67(E16)Thr→Ile, HBA2: c.203C>T]: A Novel Hemoglobin Variant That Can Be Detected by Glycated Hemoglobin Electrophoresis.
Xu AP; Chen WD; Li J; Zhou Y; Zheng RY; Li X; Ji L
Hemoglobin; 2018; 42(5-6):330-332. PubMed ID: 30612495
[TBL] [Abstract][Full Text] [Related]
26. Molecular screening of the Hbs Constant Spring (codon 142, TAA>CAA, α2) and Paksé (codon 142, TAA>TAT, α2) mutations in Thailand.
Pichanun D; Munkongdee T; Klamchuen S; Butthep P; Winichagoon P; Fucharoen S; Svasti S
Hemoglobin; 2010; 34(6):582-6. PubMed ID: 21077767
[TBL] [Abstract][Full Text] [Related]
27. Hb Stanleyville-II [α78(EF7)Asn→Lys (α2); HbA2: c.237C>A]: incidence of 1:11,500 in a newborn screening program in Brazil.
Silva MR; Sendin SM; Pimentel FS; Velloso-Rodrigues C; Romanha ÁJ; Viana MB
Hemoglobin; 2012; 36(4):388-94. PubMed ID: 22625430
[TBL] [Abstract][Full Text] [Related]
28. [Phenotypic and genotypic analysis of 45 cases with Hemoglobin Q-Thailand].
Zhong Z; Chen J; Guan Z; He H; Zhong G; Yang K
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Oct; 35(5):723-726. PubMed ID: 30298505
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. Molecular and hematological characterization of hemoglobin Hope/hemoglobin E and hemoglobin Hope/alpha-thalassemia 2 in Thai patients.
Chunpanich S; Fucharoen S; Sanchaisuriya K; Fucharoen G; Kam-itsara K
Lab Hematol; 2004; 10(4):215-20. PubMed ID: 15697092
[TBL] [Abstract][Full Text] [Related]
32. Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients.
Changtrakun Y; Fucharoen S; Ayukarn K; Siriratmanawong N; Fucharoen G; Sanchaisuriya K
Ann Hematol; 2002 Jul; 81(7):389-93. PubMed ID: 12185510
[TBL] [Abstract][Full Text] [Related]
33. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
Harteveld CL; Versteegh FG; Kok PJ; van Rooijen-Nijdam IH; van Delft P; Giordano PC
Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. [Alpha 2 codon 30 deletion (deltaGAG) causing non-deletional hemoglobin H disease in Guangxi province].
Chen P; Li SQ; Wu H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):435-9. PubMed ID: 15476164
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a new α-thalassemic hemoglobin variant found in the Iberian Peninsula: report of six cases.
Bento C; Oliveira AC; Neves J; Gameiro M; Cunha E; Coucelo M; Costa RM; Barbot J; Costa E; Fernández-Lago C; Ribeiro ML
Hemoglobin; 2012; 36(6):517-25. PubMed ID: 23181747
[TBL] [Abstract][Full Text] [Related]
38. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.
Viprakasit V; Tanphaichitr VS; Veerakul G; Chinchang W; Petrarat S; Pung-Amritt P; Higgs DR
Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697
[TBL] [Abstract][Full Text] [Related]
39. Interactions of unstable hemoglobin Rush with thalassemia and hemoglobin E result in thalassemia intermedia.
Huang K; Ge S; Yi W; Bi H; Lin K; Sun H; Huang X; Chu J; Ma S; Yang Z
Hematology; 2019 Dec; 24(1):459-466. PubMed ID: 31124399
[No Abstract] [Full Text] [Related]
40. HB ottawa [alpha 15 (A13) GLY----ARG] found in Hubei Province, People's Republic of China.
Gu YC; Wilson JB; Webber BB; Huisman TH; Wang BY; Lo YQ; Liu K; Meng B; Yuan YR
J Tongji Med Univ; 1986; 6(3):185-7. PubMed ID: 3773016
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]