126 related articles for article (PubMed ID: 34309467)
1. Hb Lepore-Hong Kong: First Report of a Novel δ/β-Globin Gene Fusion in a Chinese Family.
Jiang F; Tang XW; Li J; Zhou JY; Zuo LD; Li DZ
Hemoglobin; 2021 Jul; 45(4):220-224. PubMed ID: 34309467
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with beta(0)-thalassaemia.
So CC; Chan AY; Tsang ST; Lee AC; Au WY; Ma ES; Chan LC
Br J Haematol; 2007 Jan; 136(1):158-62. PubMed ID: 17222202
[TBL] [Abstract][Full Text] [Related]
4. Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing.
Zhuang J; Zhang N; Zheng Y; Jiang Y; Chen Y; Mao A; Chen C
Sci Rep; 2024 Apr; 14(1):9966. PubMed ID: 38693200
[TBL] [Abstract][Full Text] [Related]
5. Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China.
Jiang F; Zuo L; Li D; Li J; Tang X; Chen G; Zhou J; Lu H; Liao C
BMC Med Genet; 2020 Feb; 21(1):43. PubMed ID: 32111191
[TBL] [Abstract][Full Text] [Related]
6. Mild Thalassemia Intermedia Due to Interaction of δβ-Thalassemia with Triplicated α-Globin Genes.
Payán-Pernía S; Bernal Noguera S; Rojas Rodríguez E; Serra Ferrer M; Remacha Sevilla ÁF
Hemoglobin; 2020 Jul; 44(4):294-296. PubMed ID: 32693657
[TBL] [Abstract][Full Text] [Related]
7. Abnormal hemoglobin anti-Lepore Hong Kong compound with β
Bao X; Wang J; Qin D; Yao C; Liang J; Liang K; Du L
Sci Rep; 2024 Mar; 14(1):6682. PubMed ID: 38509195
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Identification of Three Families Carrying Hb Anti-Lepore Hong Kong Variant in Guangxi, China, and Analysis of Their Hematological Data.
Long J; Gong F; Sun L; Lai G; Chen L; Peng M; Yu C; Liu E
Hemoglobin; 2022 Nov; 46(6):325-329. PubMed ID: 36630139
[TBL] [Abstract][Full Text] [Related]
10. Detection of Hb anti-Lepore Hong Kong (NG_000007.3: g.63154_70565dup) in Chinese individuals.
Lou JW; He Y; Liu YH; Zhong BM; Zhao Y; He XX; Li DZ
Hemoglobin; 2014; 38(2):146-8. PubMed ID: 24471736
[TBL] [Abstract][Full Text] [Related]
11. Hb A2 Hong Kong - A novel δ-globin variant in a Chinese family masks the diagnosis of β-thalassemia trait.
So CC; Chan AY; Luo HY; Verhovsek M; Chui DH; Ling SC; Chan LC
Hemoglobin; 2011; 35(2):162-5. PubMed ID: 21417575
[TBL] [Abstract][Full Text] [Related]
12. New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG].
Phylipsen M; Harteveld CL; de Metz M; Gallivan MV; Arkesteijn SG; Luo HY; Chui DH; Giordano PC
Hemoglobin; 2010; 34(5):445-50. PubMed ID: 20854118
[TBL] [Abstract][Full Text] [Related]
13. An Evaluation for the Causes of Reduced Hb A
Chan NCN; Wong THY; Cheng KCK; Chan NPH; Ng MHL
Hemoglobin; 2021 Nov; 45(6):387-391. PubMed ID: 35168445
[TBL] [Abstract][Full Text] [Related]
14. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
Esteghamat F; Imanian H; Azarkeivan A; Pourfarzad F; Almadani N; Najmabadi H
Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
[TBL] [Abstract][Full Text] [Related]
15. Detection of a Hb A
Li Y; Huang T; Mao T; Zhang X; Liang L; Meng M
J Clin Lab Anal; 2020 Sep; 34(9):e23401. PubMed ID: 32770585
[TBL] [Abstract][Full Text] [Related]
16. Screening for common β-globin gene cluster deletions in Chinese individuals with increased hemoglobin F.
Cai WJ; Li J; Xie XM; Li DZ
Int J Lab Hematol; 2015 Dec; 37(6):752-7. PubMed ID: 26179971
[TBL] [Abstract][Full Text] [Related]
17. A Novel β-Thalassemia Mutation [IVS-I-6 (T>G),
Luo H; Zou Y; Liu Y
Hemoglobin; 2020 Jan; 44(1):55-57. PubMed ID: 31939318
[TBL] [Abstract][Full Text] [Related]
18. β-Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β-Thalassemia is Rare in the Indian Population.
Sreedharanunni S; Chhabra S; Hira JK; Bansal D; Sharma P; Das R
Hemoglobin; 2015; 39(5):362-5. PubMed ID: 26291970
[TBL] [Abstract][Full Text] [Related]
19. [First example of Hb lepore Washington-Boston trait in a Japanese].
Yamashiro Y; Okayama N; Sakata S; Shigedomi Y; Kawano E; Hattori Y; Ohba Y
Rinsho Byori; 1997 Dec; 45(12):1151-5. PubMed ID: 9437895
[TBL] [Abstract][Full Text] [Related]
20. Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn,
Satthakarn S; Boonmee S; Panyasai S
Hemoglobin; 2020 Nov; 44(6):385-390. PubMed ID: 33222574
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]