Glucose-6-phosphate dehydrogenase (G6PD) deficiency, abnormal haemoglobins, and thalassaemia in Yugoslavia.
Open Access
- 1 March 1966
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 3 (1) , 35-41
- https://doi.org/10.1136/jmg.3.1.35
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- MILD GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN GREEK MALESThe Lancet, 1964
- Hereditary Persistence of Fetal Hemoglobin in Greece. A Study and a ComparisonBlood, 1964
- A Thalassaemic Trait in Gipsies?Acta Medica Scandinavica, 1963
- Genetical linkage between the loci for glucose‐6‐phosphate dehydrogenase deficiency and colour‐blindness in American NegroesAnnals of Human Genetics, 1962
- [A case of thalassemia minor].1962
- [On a case of association of thalassemia and "hereditary persistence of fetal hemoglobin"].1962
- Types of Thalassaemia‐Trait Carriers as Revealed by a Study of their Incidence in GreeceBritish Journal of Haematology, 1962
- A New Hereditary Hemoglobinopathy (the Lepore Trait) and Its Interaction with Thalassemia TraitBlood, 1958
- [A case of erythroblastic hemolytic anemia of Cooley's type].1952