Homozygous βδ Thalassaemia (βδ Microcythaemia)
- 1 October 1966
- journal article
- research article
- Published by Springer Nature in Nature
- Vol. 212 (5059) , 262-264
- https://doi.org/10.1038/212262a0
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Thalassemia TraitNew England Journal of Medicine, 1964
- Controller-gene diseases: The operon model as applied to β-thalassemia, familial fetal hemoglobinemia and the normal switch from the production of fetal hemoglobin to that of adult hemoglobinJournal of Molecular Biology, 1964
- Current Concepts of the Genetics of the ThalassemiasPublished by Cold Spring Harbor Laboratory ,1964
- Trail Marking Substance of the Texas Leaf-Cutting Ant: Source and PotencyScience, 1963
- THE FUSION OF TWO PEPTIDE CHAINS IN HEMOGLOBIN LEPORE AND ITS INTERPRETATION AS A GENETIC DELETIONProceedings of the National Academy of Sciences, 1962
- α‐Thalassaemia as a Cause of Hydrops FoetalisBritish Journal of Haematology, 1962
- An improved method for the fingerprinting of human hemoglobinBiochimica et Biophysica Acta, 1961
- 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