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Volumn 137, Issue 6, 2007, Pages 489-
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Chronic and severe haemolytic anaemia caused by co-inheritance of β-thalassaemia and triplicated α-globin genes
a
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Author keywords
[No Author keywords available]
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Indexed keywords
ALPHA GLOBIN;
DEFEROXAMINE;
HEMOGLOBIN;
HEMOGLOBIN A2;
ADULT;
ARTICLE;
BETA THALASSEMIA;
BLOOD CELL COUNT;
CASE REPORT;
CHRONIC DISEASE;
DISEASE SEVERITY;
ERYTHROCYTE COUNT;
GENE MUTATION;
HEMOLYTIC ANEMIA;
HEREDITY;
HETEROZYGOSITY;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
HUMAN;
IRON CHELATION;
IRON OVERLOAD;
LEUKOCYTE COUNT;
LIQUID CHROMATOGRAPHY;
MALE;
MICROCYTOSIS;
PHENOTYPE;
PRIORITY JOURNAL;
RETICULOCYTE COUNT;
SPLENOMEGALY;
THROMBOCYTE COUNT;
ADULT;
ANEMIA, HEMOLYTIC;
BETA-THALASSEMIA;
CHRONIC DISEASE;
GENE DOSAGE;
GLOBINS;
HETEROZYGOTE;
HUMANS;
MALE;
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EID: 34249304788
PISSN: 00071048
EISSN: 13652141
Source Type: Journal
DOI: 10.1111/j.1365-2141.2007.06575.x Document Type: Article |
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Times cited : (3)
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References (0)
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