Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children [letter]-Reference-Cited by-同舟云学术

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Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children [letter]

Published:1993-10-15 Issue:8 Volume:82 Page:2595-2596
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

de Montalembert M,Maier-Redelsperger M,Girot R,Belloy M,Vilmer E,Ducrocq R,Guidal C,Elion J

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/82/8/2595/612193/2595b.pdf

Cited by 10 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. Genetic Variation and Sickle Cell Disease Severity;JAMA Network Open;2023-10-18

2. Variability of homozygous sickle cell disease: The role of alpha and beta globin chain variation and other factors;Blood Cells, Molecules, and Diseases;2018-05

3. Alpha-thalassaemia promotes frequent vaso-occlusive crises in children with sickle cell anaemia through haemorheological changes;Pediatric Blood & Cancer;2017-01-18

4. Comment on “Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia”;Revista Brasileira de Hematologia e Hemoterapia;2014-09

5. Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia;British Journal of Haematology;2013-08

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