THALASSAEMIA SYNDROMES - GENETIC STUDIES ON THALASSAEMIA MINOR WITH LARGE AMOUNTS OF FETAL HAEMOGLOBIN
- 1 January 1965
- journal article
- research article
- Vol. 14 (2-3) , 79-+
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Thalassemia TraitNew England Journal of Medicine, 1964
- The First Observation of Homozygous Hemoglobin S-Alpha Thalassemia Disease and Two Types of Sickle Cell Thalassemia Disease: (a) Sickle Cell-Alpha Thalassemia Disease, (b) Sickle Cell-Beta Thalassemia DiseaseBlood, 1963
- Reciprocal Relationship of Hemoglobins A2 and F in Beta Chain Thalassemias, a Key to the Genetic Control of Hemoglobin FBlood, 1961
- The Thalassaemia SyndromesActa Haematologica, 1961
- Genetic Basis of the Thalassæmia DiseasesNature, 1959
- Starch Block Electrophoretic Studies of Human Hemoglobin Solutions II. Results in Cord Blood, Thalassemia and other Hematologic Disorders: Comparison with Tiselius ElectrophoresisBlood, 1958
- Zone electrophoresis in starch gels: group variations in the serum proteins of normal human adultsBiochemical Journal, 1955