References
- Heipel M, Wendt F. Congenital dyserythropoietic anaemia with karyorrhexis and multinuclearity of erythroblasts. Helv Med Acta 1968; 103–15
- Crookston J H, Crookston M C, Burnie KL, et al. Hereditary erythroblastic multinuclearity associated with a positive acidified serum test: a type of CDA. Br J Haematol 1969; 17: 11–26
- Borst-Eilers E, Moes M, Nijessen JG. A CDA Type II family with a weak or variant HEMPAS antigen. Third Meeting, European and African Division, International Society of Haematology. London 1975; 27: 7, Abstract
- Hruby M A, Mason R G, Honig GR. Unbalanced globin chain synthesis in congenital dyserythropoietic anemia. Blood 1973; 42: 843–50
- Weatherall D J, Clegg J B, Knox-Macaulay H HM, et al. A genetically determined disorder with features both of thalassaemia and congenital dyserythropoietic anaemia. Br J Haematol 1973; 24: 681–702
- Weatherly T L, Flannery E P, Doyle WF, et al. Congenital dyserythropoietic anemia with increased red cell lipids. Am J Med 1974; 57: 912
- Ventura A, Panizon F, Soranzo MR, et al. Congenital dyserythropoietic anaemia Type II associated with a new type of G-6PD deficiency (G-6PD Gabrovizza). Acta Haematol 1984; 71: 227–34
- Dacie J V, Lewis SM. Practical Haematology. Churchill Livingstone., Edinburgh 1975
- Verwilghen R L, Lewis S M, Dacie JV, et al. HEMPAS: Congenital dyserythropoietic anaemia (Type II). Quarterly J Med 1973; 42: 257–18
- Chan T K, Todd D, Tso SC. Drug induced haemolysis in glucose-6-phosphate dehydrogenase deficiency. Br Med J 1976; 2: 1227–9
- Chan CK. Measurement of erythrocyte glucose-6-phosphate dehydrogenase activity using a centrifugal analyser. Med Lab Sci 1984; 41: 112–20
- Alloisio N, Jaccond P, Dorleac E. Alterations of globin chain synthesis and of red cell membrane proteins in congenital dyserythropoietic anemia I and II. Pediatr Res 1982; 16: 1016–21