Journal article
Laboratory diagnosis of HB CC-α-thalassemia
Abstract
Routine laboratory investigations of hemoglobinopathies include Hb electrophoresis for abnormal hemoglobins, determination of Hb A2 (alpha 2 delta 2) for beta-thalassemia traits, staining for Hb H (beta 4) inclusions for alpha-thalassemia traits and estimation of Hb F (alpha 2 lambda 2) for the presence of hereditary persistence of fetal hemoglobin genes (HPFH). Frequently, analytical column chromatography and alpha/beta hemoglobin chain …
Authors
Wong SC; Ali MAM
Journal
Clinical Biochemistry, Vol. 12, No. 5, pp. 157–158
Publisher
Elsevier
Publication Date
10 1979
DOI
10.1016/s0009-9120(79)80080-6
ISSN
0009-9120