REFERENCES
- Giordano P. C. Hemoglobinopathieàn in Nederland. Dignostiek, Epidemiologie en Preventie. 1998, ISBN 90-9011949-3.
- Giordano P. C., van Delft P., Batelaan D., Harteveld C. L., Bernini L. F. Hemoglobinopathy Analyses in The Netherlands: A Report of an In Vitro Globin Chain Biosynthesis Survey Using a Rapid, Modified Method. Clin. Lab. Haem. 1999; 21: 247–255
- Harteveld C. L., Losekoot M., Haak H., Heister J.G. A.M., Giordano P. C., Bernini L. F. A Novel Polyadenyation Signal Mutation in the α2-Globin Gene Causing Thalassaemia. Br. J. Haematol. 1994; 87: 139–143
- Kattamis A. C., Camaschella C., Sivera P., Surrey S., Fortina P. Human α Thalassemia Syndromes: Detection of Molecular Defects. Am. J. Hematol 1996; 53: 81–91
- Chong S. S., Boehm C. D., Higgs D. R., Cutting G. R. Single-Tube Multiplex-PCR Screening for Common Deletion Determinants of α-Thalassemia. Blood 2000; 95: 360–362
- Wajcman H., Kister J., Promé D., Blouquit Y., Préhu C., Poyart C., Galactéros F. Interaction of Two Amino Acid Substitutions within the Same β Chain of Human Hemoglobin: the Examples of Hb Corbeil [β26(B8)Glu→Lys, β104(G6)Arg→Thr] and Hb Villeparisis [β77(EF1)His→Tyr, β80(EF4)Asn→Ser]. Comptes Rendus Acad. Sci. Paris, Sciences de La Vie/Life Sciences 1995; 318: 785–794
- HbVar Database on Abnormal Hemoglobins (http://globin.cse.psu.edu).
- Préhu C., Riou J., Godart C., Bost M., Barro C., Prome D., Kister J., Galacteros F., Wajcman H. Hb Diamant [α119(H2)Pro→Leu]: a New Variant With a Modification at the α1β1 Interface. Hemoglobin 2000; 24(3)249–252
- Wickramasinghe S. N., Lee M. J. Evidence That the Ubiquitin Proteolytic Pathway is Involved in the Degradation of Precipitated Globin Chains in Thalassaemia. Br. J. Haematol. 1998; 101: 245–250