THE PRESENT STATUS OF THE HETEROGENEITY OF FETAL HEMOGLOBIN IN β‐THALASSEMIA: AN ATTEMPT TO UNIFY SOME OBSERVATIONS IN THALASSEMIA AND RELATED CONDITIONS*
- 1 May 1974
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 232 (1) , 107-124
- https://doi.org/10.1111/j.1749-6632.1974.tb20576.x
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- A Second Type of Hereditary Persistence of Foetal Haemoglobin in IndiaBritish Journal of Haematology, 1973
- δβ-Thalassaemia in a Chinese FamilyBritish Journal of Haematology, 1972
- A Homozygote for the HbGγType of Foetal Haemoglobin in India: A Study of Two Indian and Four Negro FamiliesBritish Journal of Haematology, 1972
- Nature of Foetal Haemoglobin in F-ThalassaemiaBritish Journal of Haematology, 1971
- GAMMA-THALASSÆMIAThe Lancet, 1971
- Nature of fetal hemoglobin in the Greek type of hereditary persistence of fetal hemoglobin with and without concurrent β-thalassemiaJournal of Clinical Investigation, 1970
- HEMOGLOBIN S‐THALASSEMIA SYNDROME IN NEGRO CHILDREN1Annals of the New York Academy of Sciences, 1969
- EVIDENCE FOR MULTIPLE STRUCTURAL GENES FOR THE GAMMA‐CHAIN OF HUMAN FETAL HEMOGLOBIN IN HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN*Annals of the New York Academy of Sciences, 1969
- Homozygous βδ Thalassaemia (βδ Microcythaemia)Nature, 1966
- Genetic and Biochemical Studies of‘Intermediate’Types of Cooley's Anaemia*British Journal of Haematology, 1955