Thalassemia—Hemoglobin C Disease
Open Access
- 1 November 1954
- journal article
- research article
- Published by American Society of Hematology in Blood
- Vol. 9 (11), 1047-1054
- https://doi.org/10.1182/blood.v9.11.1047.1047
Abstract
An unusual type of severe chronic hypochromic microcytic anemia in a Negro is described and attributed to the interaction of the hemoglobin C gene with the thalassemia gene. The patient and his father were shown to be carriers of the C trait, the mother and several siblings of the thalassemia gene.This publication has 8 references indexed in Scilit:
- SideroblastsBlood, 1954
- Further Studies on Hemoglobin CBlood, 1953
- Two Cases of Sickle Cell Disease Presumably Due to the Combination of the Genes for Thalassemia and Sickle Cell HemoglobinBlood, 1953
- Genetic Aspects of Sickle Cell Anemia and Microdrepanocytic DiseaseBlood, 1952
- A New Inherited Abnormality of Hemoglobin and Its Interaction with Sickle Cell HemoglobinBlood, 1951
- THE OCCURRENCE IN A FAMILY OF SICILIAN ANCESTRY OF THE TRAITS FOR BOTH SICKLING AND THALASSEMIABlood, 1950
- MEDITERRANEAN HEMOPATHIC SYNDROMESBlood, 1949
- HEMATOLOGIC AND GENETIC STUDY OF THE TRANSMISSION OF THALASSEMIAArchives of Internal Medicine, 1944