Clinical features and molecular analysis of acquired hemoglobin H disease
- 1 August 1983
- journal article
- research article
- Published by Elsevier in The American Journal of Medicine
- Vol. 75 (2) , 181-191
- https://doi.org/10.1016/0002-9343(83)91189-0
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- Detection of specific sequences among DNA fragments separated by gel electrophoresisPublished by Elsevier ,2006
- The chromosomal arrangement of human α-like globin genes: Sequence homology and α-globin gene deletionsCell, 1980
- Determination of Alpha Thalassaemia Phenotypes by Messenger RNA AnalysisBritish Journal of Haematology, 1980
- Acquired Haemoglobin H Disease in Leukaemia: Pathophysiology and Molecular BasisBritish Journal of Haematology, 1978
- Molecular basis for acquired haemoglobin H diseaseNature, 1977
- Reliable routine estimation of small amounts of foetal haemoglobin by alkali denaturation.Journal of Clinical Pathology, 1972
- The Pattern of Disordered Haemoglobin Synthesis in Homozygous and Heterozygous β-ThalassaemiaBritish Journal of Haematology, 1969
- Abnormal human haemoglobins: Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb chesapeake and Hb J (Bangkok)Journal of Molecular Biology, 1966
- An Unstable Haemoglobin Associated with Some Cases of LeukaemiaBritish Journal of Haematology, 1960
- Estimation of Small Percentages of Fœtal HæmoglobinNature, 1959