An Egyptian β-thalassaemia heterozygote with normal haemoglobins A2 and F: A problem in population screening
Open Access
- 12 February 2009
- journal article
- research article
- Published by Springer Nature in Hereditas
- Vol. 95 (1) , 149-153
- https://doi.org/10.1111/j.1601-5223.1981.tb01333.x
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Haemoglobin El Faiyum-Possibly an Egyptian haemoglobin DHereditas, 2009
- Characterisation of deletions which affect the expression of fetal globin genes in manNature, 1979
- The Heterogeneity of Normal Hb A2‐β Thalassaemia in GreeceBritish Journal of Haematology, 1979
- Chromosomal localization of human β globin gene on human chromosome 11 in somatic cell hybridsProceedings of the National Academy of Sciences, 1978
- Localization of the human α-globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridization assayCell, 1977
- Thalassemias, Abnormal Hemoglobins and Glucose‐6‐Phosphate Dehydrogenase Deficiency in the Arta Area of Greece: Diagnostic and Genetic Aspects of Complete Village Studies*Annals of the New York Academy of Sciences, 1964
- Types of Thalassaemia‐Trait Carriers as Revealed by a Study of their Incidence in GreeceBritish Journal of Haematology, 1962
- Observations on the Minor Basic Hemoglobin Component in the Blood of Normal Individuals and Patients with ThalassemiaJournal of Clinical Investigation, 1957
- Demonstration von fetalem H moglobin in den Erythrocyten eines BlutausstrichsJournal of Molecular Medicine, 1957
- The determination of iron in blood plasma or serumClinica Chimica Acta; International Journal of Clinical Chemistry, 1957