The diagnosis of beta-thalassemia trait: A review
- 1 January 1976
- journal article
- review article
- Published by Wiley in American Journal of Hematology
- Vol. 1 (1) , 129-137
- https://doi.org/10.1002/ajh.2830010115
Abstract
Diagnostic and screening methods for beta‐thalassemia trait are reviewed in the order of their development, including identification by homozygous offspring, erythrocyte morphology, osmotic fragility, hemoglobin composition, globin synthetic rates, and red blood cell indices.Keywords
This publication has 39 references indexed in Scilit:
- RED-CELL-VOLUME DISTRIBUTION CURVES AND THE MEASUREMENT OF ANISOCYTOSISThe Lancet, 1974
- Immunological quantification of hemoglobins F and A2Clinica Chimica Acta; International Journal of Clinical Chemistry, 1974
- DIFFERENTIATION OF IRON DEFICIENCY FROM THALASSÆMIA TRAITThe Lancet, 1973
- DIFFERENTIATION OF IRON DEFICIENCY FROM THALASSÆMIA TRAIT BY ROUTINE BLOOD-COUNTThe Lancet, 1973
- CorrespondenceBlood, 1972
- High Concentrations of Haemoglobin A2 in Malaria PatientsNature, 1967
- Abnormal human haemoglobins: Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb chesapeake and Hb J (Bangkok)Journal of Molecular Biology, 1966
- L'emoglobina normale lenta A2: suoi rapporti con una nuova frazione emoglobinica lenta, B2, e sua importanza per il riconoscimento di varianti talassemiche che compaiono nelle famiglie di portatori di Thalassemia media e di emoglobinopatia HActa geneticae medicae et gemellologiae, 1959
- FAMILIAL MEDITERRANEAN TARGET???OVAL CELL SYNDROMESThe Lancet Healthy Longevity, 1943
- ???TARGET CELL??? ANEMIAThe Lancet Healthy Longevity, 1940