DIAGNOSIS OF BETA THALASSAEMIA IN THE NEWBORN BY MEANS OF HAEMOGLOBIN SYNTHESIS
- 1 September 1970
- journal article
- Published by Wiley in Acta Paediatrica
- Vol. 59 (5) , 523-528
- https://doi.org/10.1111/j.1651-2227.1970.tb16802.x
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- The Correlation between Red-Cell Survival and Excess of α-Globin Synthesis in β-ThalassaemiaBritish Journal of Haematology, 1969
- Absence of β-Globin Synthesis and Excess of α-Globin Synthesis in Homozygous β-Thalassaemic Subjects from the Ferrara RegionNature, 1968
- Excess α Chain Synthesis Relative to β Chain Synthesis in Thalassaemia Major and MinorNature, 1966
- Rapid Qualitative and Quantitative Hemoglobin Fractionation: Cellulose Acetate ElectrophoresisAmerican Journal of Clinical Pathology, 1965
- Globin Synthesis in Thalassaemia: An in vitro StudyNature, 1965
- Observations on the Chromatographic Heterogeneity of Normal Adult and Fetal Human Hemoglobin: A Study of the Effects of Crystallization and Chromatography on the Heterogeneity and Isoleucine ContentJournal of the American Chemical Society, 1958
- Studies on Abnormal HemoglobinsBlood, 1951