标题
Fetal hemoglobin in sickle cell anemia
作者
关键词
-
出版物
BLOOD
Volume 118, Issue 1, Pages 19-27
出版商
American Society of Hematology
发表日期
2011-04-14
DOI
10.1182/blood-2011-03-325258
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- National Institutes of Health Consensus Development Conference Statement: Hydroxyurea Treatment for Sickle Cell Disease
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- Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of -thalassemia
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- DNA polymorphisms at the BCL11A, HBS1L-MYB, and -globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease
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- Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific RepressorBCL11A
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- Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations
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