Hereditary Persistence of Foetal Haemoglobin Production, and its Interaction with the Sickle‐Cell Trait
- 1 April 1958
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 4 (2), 138-149
- https://doi.org/10.1111/j.1365-2141.1958.tb03844.x
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- STUDIES ON THE DESTRUCTION OF RED BLOOD CELLS. XII. FACTORS INFLUENCING THE ROLE OF S HEMOGLOBIN IN THE PATHOLOGIC PHYSIOLOGY OF SICKLE CELL ANEMIA AND RELATED DISORDERS 1Journal of Clinical Investigation, 1957
- A Study of the Survival Rate of Cases of Sickle-cell AnaemiaBMJ, 1957
- Sickle-cell--Thalassaemia Disease in South TurkeyBMJ, 1957
- Estimation of Small Proportions of Fœtal Hæmoglobin in BloodNature, 1956
- THE ABNORMAL HUMAN HEMOGLOBINSMedicine, 1956
- Sickle-cell GeneBMJ, 1955
- A Family Illustrating the Double Inheritance of the Sickle Cell Trait and of Mediterranean AnaemiaJournal of Clinical Pathology, 1954
- Serum Iron and Iron-binding Capacity in the South African BantuNature, 1953
- Sickle Cell Anemia, a Molecular DiseaseScience, 1949
- The Inheritance of Sickle Cell AnemiaScience, 1949