Complex interaction of Hb Q-Thailand and Hb E with α0-thalassemia and hereditary persistence of fetal hemoglobin in a Chinese family-Reference-Cited by-同舟云学术

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Complex interaction of Hb Q-Thailand and Hb E with α0-thalassemia and hereditary persistence of fetal hemoglobin in a Chinese family

Published:2010-03-24 Issue:9 Volume:89 Page:883-888
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Zheng Weidong,Liu Yanhui,Chen Dong,Rong Kabin,Ge Yanfen,Gong Caiping,Chen Heping

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00277-010-0935-z.pdf

Reference23 articles.

1. Zeng FY, Fucharoen S, Huang SZ, Rodgers GP (1992) Hb Q-Thailand [α74(EF3)Asp → His]: gene organization, molecular structure, and DNA diagnosis. Hemoglobin 16:481–491

2. Fucharoen S, Winichagoon P (2000) Clinical and hematologic aspects of hemoglobin E beta-thalassemia. Curr Opin Hematol 7:106–112

3. Zeng YT, Huang SZ (1987) Disoreders of haemoglobin in China. J Med Genet 24:578–583

4. Beris P, Huber P, Miescher PA, Wilson JB, Kutlar A, Chen SS et al (1987) Hb Q-Hb H disease in a Chinese living in Geneva, Switzerland: characterization of the variant and identification of the two alpha-thalassemic chromosomes. Am J Hematol 24:395–400

5. Li D, Liao C, Xie X, Zhong H, Li J (2007) Four cases of Hb Q-H disease found in Southern China. Hemoglobin 31:109–111

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. β-thalassemia caused by compound heterozygous mutations and cured by bone marrow transplantation: A case report;Molecular Medicine Reports;2017-05

2. Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family;Hemoglobin;2017-01-02

3. Genetic heterogeneity of hemoglobin AEBart's disease: A large cohort data from a single referral center in northeast Thailand;Blood Cells, Molecules, and Diseases;2014-04

4. Five Hemoglobin Variants in a Double Heterozygote for α- and β-Globin Chain Defects;Acta Haematologica;2013-09-24

5. Incidence of haemoglobin E and α-thalassaemia mutations and their interaction among the tribal populations of Assam and Arunachal Pradesh in North Eastern India;The Nucleus;2013-07-17

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