Modifier genes and sickle cell anemia
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology
Reference57 articles.
1. Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia
2. Concordant fetal hemoglobin response to hydroxyurea in siblings with sickle cell disease
3. Evidence of Genetic Interaction between the β-Globin Complex and Chromosome 8q in the Expression of Fetal Hemoglobin
4. An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age
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3. Sleep disordered breathing and its relation to stroke and pulmonary hypertension in children with sickle cell disease: a single-center cross-sectional study;Annals of Hematology;2023-01-16
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5. Influence of Oxidative Stress Biomarkers and Genetic Polymorphisms on the Clinical Severity of Hydroxyurea-Free Senegalese Children with Sickle Cell Anemia;Antioxidants;2020-09-14
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