Acquired Haemoglobin H Disease in Leukaemia: Pathophysiology and Molecular Basis
- 12 March 1978
- journal article
- research article
- Published by Wiley in British Journal of Haematology
- Vol. 38 (3), 305-322
- https://doi.org/10.1111/j.1365-2141.1978.tb01049.x
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- Deletion of α-globin genes in haemoglobin-H disease demonstrates multiple α-globin structural lociNature, 1975
- Kinetic studies of gene frequency: I. Use of a DNA copy of reticulocyte 9 S RNA to estimate globin gene dosage in mouse tissuesJournal of Molecular Biology, 1974
- DNA Sequences Neighboring the Duck Hemoglobin GenesPublished by Cold Spring Harbor Laboratory ,1974
- Controlled fragmentation of DNA by DNase IAnalytical Biochemistry, 1972
- Purification of Biologically Active Globin Messenger RNA by Chromatography on Oligothymidylic acid-CelluloseProceedings of the National Academy of Sciences, 1972
- Acquired Hemoglobin H DiseaseNew England Journal of Medicine, 1971
- 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
- Occurrence of Hæmoglobin H in LeukæmiaNature, 1963
- Estimation of Small Percentages of Fœtal HæmoglobinNature, 1959
- Observations on the Chromatographic Heterogeneity of Normal Adult and Fetal Human Hemoglobin: A Study of the Effects of Crystallization and Chromatography on the Heterogeneity and Isoleucine ContentJournal of the American Chemical Society, 1958