High prevalence of individuals with low concentration of fetal hemoglobin in F‐cells in sickle cell anemia in Tanzania
Open Access
- 16 April 2016
- journal article
- other
- Published by Wiley in American Journal of Hematology
- Vol. 91 (8) , E323-E324
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Genetic variants at HbF‐modifier loci moderate anemia and leukocytosis in sickle cell disease in TanzaniaAmerican Journal of Hematology, 2014
- Fetal hemoglobin in sickle cell anemia: a glass half full?Blood, 2014
- Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimatesThe Lancet, 2013
- Foetal Haemoglobin, Erythrocytes Containing Foetal Haemoglobin, and Hematological Features in Congolese Patients with Sickle Cell AnaemiaAnemia, 2012
- Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea. Multicenter Study of Hydroxyurea.1997
- X-LINKED DOMINANT CONTROL OF F-CELLS IN NORMAL ADULT LIFE - CHARACTERIZATION OF THE SWISS TYPE AS HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN REGULATED DOMINANTLY BY GENE(S) ON X-CHROMOSOME1988
- X-linked dominant control of F-cells in normal adult life: characterization of the Swiss type as hereditary persistence of fetal hemoglobin regulated dominantly by gene(s) on X chromosomeBlood, 1988