Prenatal Diagnosis of Thalassemia and Hb S Syndromes in Greece: An Evaluation of 1500 Cases
- 1 June 1985
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 445 (1) , 357-375
- https://doi.org/10.1111/j.1749-6632.1985.tb17206.x
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Antenatal Diagnosis of Thalassemia: A ReviewaAnnals of the New York Academy of Sciences, 1985
- Prenatal diagnosis of thalassaemia by haemoglobin chromatography on biorex an evaluation of the methodPrenatal Diagnosis, 1984
- Antenatal diagnosis of haemoglobinopathies by Biorex chromatography of haemoglobinBritish Journal of Haematology, 1982
- PRENATAL DIAGNOSIS OF HAEMOGLOBINOPATHIES: A STATUS REPORTThe Lancet, 1981
- Base substitution in an intervening sequence of a beta+-thalassemic human globin gene.Proceedings of the National Academy of Sciences, 1981
- Prenatal diagnosis of hemoglobinopathies: comparison of the results obtained by isoelectric focusing of hemoglobins and by chromatography of radioactive globin chainsBlood, 1980
- Prenatal Diagnosis of HemoglobinopathiesNew England Journal of Medicine, 1976
- Enrichment of erythrocytes of fetal origin from adult-fetal blood mixtures via selective hemolysis of adult blood cells: an aid to antenatal diagnosis of hemoglobinopathiesBlood, 1976
- INTRAUTERINE DIAGNOSIS OF THALASSEMIAAnnals of the New York Academy of Sciences, 1974
- 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