These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
155 related articles for article (PubMed ID: 24826791)
1. Screening and diagnosis of Hb Quong Sze [HBA2: c.377T > C (or HBA1)] in a prenatal control program for thalassemia. Yang Y; Lou JW; Liu YH; He Y; Li DZ Hemoglobin; 2014; 38(3):158-60. PubMed ID: 24826791 [TBL] [Abstract][Full Text] [Related]
2. Molecular analysis and clinical significance of hemoglobin Quong Sze in Huizhou city, Southern China. Zhong Z; Guan Z; Chen D; Zhong G; He H; Yang K; Chen J Taiwan J Obstet Gynecol; 2023 Sep; 62(5):709-712. PubMed ID: 37678999 [TBL] [Abstract][Full Text] [Related]
3. Identification of nondeletional α-thalassemia in a prenatal screening program by reverse dot-blot in southern China. Li J; Li R; Li DZ Hemoglobin; 2015; 39(1):42-5. PubMed ID: 25523870 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Comparison of the effect of three β-thalassemia prenatal screening strategies using in Guangdong province]. Li B; Yin A; Luo M; Wu L; Ma Y; Wang X; Zhang X; Zhao Q Zhonghua Fu Chan Ke Za Zhi; 2015 Jun; 50(6):434-40. PubMed ID: 26311551 [TBL] [Abstract][Full Text] [Related]
7. Hematological Characteristics of Hb Constant Spring ( Jiang F; Xu LL; Chen GL; Zhou JY; Li J; Tang XW; Zuo LD; Li DZ Hemoglobin; 2020 Mar; 44(2):86-88. PubMed ID: 32338097 [TBL] [Abstract][Full Text] [Related]
8. Prenatal control of nondeletional α-thalassemia: first experience in mainland China. Li J; Li R; Zhou JY; Xie XM; Liao C; Li DZ Prenat Diagn; 2013 Sep; 33(9):869-72. PubMed ID: 23637094 [TBL] [Abstract][Full Text] [Related]
9. Population Screening and Prevention Strategies for Thalassemias and other Hemoglobinopathies of Eastern India: Experience of 18,166 cases. Chatterjee T; Chakravarty A; Chakravarty S Hemoglobin; 2015; 39(6):384-8. PubMed ID: 26428539 [TBL] [Abstract][Full Text] [Related]
10. alpha-thalassemia-2 and the variability of hematological values in children with sickle cell anemia. Altay C; Gravely ME; Joseph BR; Williams DF Pediatr Res; 1981 Aug; 15(8):1093-6. PubMed ID: 7267182 [TBL] [Abstract][Full Text] [Related]
11. The Hb E (HBB: c.79G>A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/- - Leckngam P; Limweeraprajak E; Kiewkarnkha T; Tatu T Hemoglobin; 2017 Jan; 41(1):38-43. PubMed ID: 28413893 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Effective screening for double heterozygosity of Hb E/alpha0-thalassemia. Sanchaisuriya K; Chirakul S; Srivorakun H; Fucharoen G; Fucharoen S; Changtrakul Y; Sanchaisuriya P Ann Hematol; 2008 Nov; 87(11):911-4. PubMed ID: 18575861 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Evaluation of intervention strategy of thalassemia for couples of childbearing ages in Centre of Southern China. Jiang F; Zuo L; Li J; Chen G; Tang X; Zhou J; Qu Y; Li D; Liao C J Clin Lab Anal; 2021 Oct; 35(10):e23990. PubMed ID: 34492731 [TBL] [Abstract][Full Text] [Related]
16. A Novel Mutation of the α2-Globin Gene Causing α Chen B; Lin L; Yi S; Chen Q; Wei H; Li G; Zheng C; He S; Qiu X Hemoglobin; 2017 Jan; 41(1):56-58. PubMed ID: 28395547 [TBL] [Abstract][Full Text] [Related]
17. Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden ( Du L; Bao X; He W; Qin D; Wang J; Xiong Y; Shi X; Ding H; Yao C; Wu J J Int Med Res; 2021 Jul; 49(7):3000605211031429. PubMed ID: 34334003 [TBL] [Abstract][Full Text] [Related]
18. Erythrocyte Indices and Hemoglobin Analysis for α-Thalassemia Screening in an Area with High Carrying Rate. Zheng L; Huang H; Wu X; Shen Q; Chen M; Wang M; Su L; Xu L Indian J Hematol Blood Transfus; 2022 Apr; 38(2):352-358. PubMed ID: 35496953 [TBL] [Abstract][Full Text] [Related]
19. Third-generation sequencing identified two rare α-chain variants leading to hemoglobin variants in Chinese population. Zhuang J; Jiang Y; Chen Y; Mao A; Chen J; Chen C Mol Genet Genomic Med; 2024 Jan; 12(1):e2365. PubMed ID: 38284449 [TBL] [Abstract][Full Text] [Related]
20. [Clinical and molecular characteristics of hemoglobin New York in Guangxi populations]. Li YQ; Huang HP; Yang WH; Chen ZZ; Zhao L; Huang HY; Qin GF Zhonghua Xue Ye Xue Za Zhi; 2013 Aug; 34(8):696-9. PubMed ID: 23978022 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]