DUPLICATION OF ALPHA-THALASSÆMIA GENE IN THREE GREEK FAMILIES WITH HÆMOGLOBIN H DISEASE
- 26 September 1970
- journal article
- Published by Elsevier in The Lancet
- Vol. 296 (7674) , 635-637
- https://doi.org/10.1016/s0140-6736(70)91401-7
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- DIFFERENT TYPES OF ALPHA-THALASSÆMIA AND SIGNIFICANCE OF HÆMOGLOBIN BART'S IN NEONATESThe Lancet, 1970
- The Genetical Interpretation of Haemoglobin H DiseaseHuman Heredity, 1970
- UNBALANCED GLOBIN CHAIN SYNTHESIS IN ALPHA-THALASSEMIA HETEROZYGOTESAnnals of the New York Academy of Sciences, 1969
- Differences between - and -Chain Mutants of Human Haemoglobin and between - and -Thalassaemia. Possible Duplication of the -Chain GeneBMJ, 1968
- Studies on haemoglobin Bart's (Hb??4) in Thailand: the incidence and the mechanism of occurrence in cord blood*Annals of Human Genetics, 1967
- Hæmoglobin H Disease in Thailand: a Genetical StudyNature, 1964
- α‐Thalassaemia as a Cause of Hydrops FoetalisBritish Journal of Haematology, 1962
- Genetics of haemoglobin HAnnals of Human Genetics, 1961