δβ Thalassemia and Hereditary Persistence of Fetal Hemoglobin
Open Access
- 1 June 1991
- journal article
- Published by Elsevier in Hematology/Oncology Clinics of North America
- Vol. 5 (3) , 399-422
- https://doi.org/10.1016/s0889-8588(18)30422-2
Abstract
No abstract availableKeywords
This publication has 91 references indexed in Scilit:
- The DNA deletion in an Indian δβ‐thalassaemia begins one kilobase from the Aγ globin gene and ends in an LI repetitive sequenceBritish Journal of Haematology, 1989
- The greekaγβ+‐hpfh observed in a large black familyAmerican Journal of Hematology, 1987
- (Aγδβ)°‐Thalassaemia in Blacks is due to a deletion of 34 kbp of DNABritish Journal of Haematology, 1985
- Characterization of an Indian (δβ)° thalassaemiaBritish Journal of Haematology, 1984
- The deletion in a type of δ0-β0-thalassaemia begins in an inverted AluI repeatNature, 1982
- A gene deletion ending at the midpoint of a repetitive DNA sequence in one form of hereditary persistence of fetal haemoglobinNature, 1982
- Linkage Analysis of Nondeletion Hereditary Persistence of Fetal HemoglobinScience, 1982
- Major rearrangement in the human β-globin gene clusterNature, 1981
- Heterogeneity in the molecular basis of hereditary persistence of fetal haemoglobinNature, 1980
- Globin Chain Synthesis in the Greek Type (Aγ) of Hereditary Persistence of Fetal HaemoglobinBritish Journal of Haematology, 1975