Prenatal diagnosis of β thalassaemia by reverse phase HPLC
- 1 March 1987
- journal article
- research article
- Published by Wiley in Prenatal Diagnosis
- Vol. 7 (3) , 171-178
- https://doi.org/10.1002/pd.1970070304
Abstract
Reverse phase HPLC of radioactive globin chains has been compared to classical carboxy methyl cellulose chromatography for the prenatal diagnosis of β thalassaemia. The two methods correlated highly (r = 0.97 p < 0.0005) and provided an identical diagnosis for 40 fetal blood samples of fetuses homozygous or heterozygous for β thalassaemia. The HPLC procedure was much faster and required fewer biochemical steps (no globin preparation). It was at least as accurate and more sensitive than the classical chromatography. A single column can be used for 150 analyses and is always ready to be used. Last but not least it is much less expensive than CMC chromatography.Keywords
This publication has 19 references indexed in Scilit:
- Antenatal diagnosis of haemoglobinopathies by improved method of isoelectric focusing of haemoglobinsBritish Journal of Haematology, 1984
- Prenatal diagnosis of thalassaemia by haemoglobin chromatography on biorex an evaluation of the methodPrenatal Diagnosis, 1984
- Prenatal Diagnosis of Sickle-Cell Anemia in the First Trimester of PregnancyNew England Journal of Medicine, 1983
- Antenatal diagnosis of haemoglobinopathies by Biorex chromatography of haemoglobinBritish Journal of Haematology, 1982
- DIFFICULTIES IN ANTENATAL DIAGNOSIS OF INHERITED HAEMOGLOBINOPATHIES: γ-CHAIN VARIANTSBritish Journal of Haematology, 1981
- Globin Chain Electrophoresis for Prenatal Diagnosis of β ThalassemiaHemoglobin, 1981
- Isoelectric Focusing of Globin Chains for Antenatal Diagnosis of β°-ThalassemiaHemoglobin, 1981
- Prenatal Diagnosis of HemoglobinopathiesNew England Journal of Medicine, 1976
- FETAL BLOOD-SAMPLING IN UTEROThe Lancet, 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