Differences in response to fetal hemoglobin induction therapy in β-thalassemia and sickle cell disease
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference23 articles.
1. Pathogenesis and treatment of sickle cell disease;Bunn;N. Engl. J. Med.,1997
2. Pathophysiology of thalassaemia;Weatherall;Bailliere's Clin. Haematol.,1998
3. Fetal haemoglobin and early manifestations of homozygous sickle cell disease;Bailey;Arch. Dis. Child.,1992
4. Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood;Stevens;J. Pediatr.,1981
5. Delta beta thalassemia and hereditary persistence of fetal hemoglobin;Bollekens;Hematol./Oncol. Clin. North Am.,1991
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