Mobilization of peripheral blood progenitor cells with G-CSF alone in lymphoma patients: steady-state circulating progenitor cell count predicts the autograft yield.

1994. p. 157. 2. Kulozik AE. -thalassaemia: molecular pathogenesis and clinical variability. Eur J Pediatr 1992; 151:78-84. 3. Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988; 16:1215. 4. Old JM, Varawalla NY, Weatherall DJ. Rapid detection and prenatal diagnosis of -thalassaemia: studies in Indian and Cypriot populations in the UK. Lancet 1990; 336:834-7. 5. Roldán A, Gutiérrez M, Cygler A, et al. Molecular characterization of -thalassemia genes in an Argentine population. Am J Hematol 1997; 54:179-82. 6. Soria NW, Tulián CL, Plassa F, Roth GA. -thalassemia and hemoglobin types in Argentina: determination of most frequent mutations. Am J Hematol 1997; 54:160-3. 7. Noguera N, Bragós I, Morisoli L, Milani A. Screening for hemoglobinopathies in neonates in Argentina. Haematologica 1999; 84:387-9. 8. Schiliró G, Di Gregorio F, Samperi P, et al. Genetic heterogeneity of thalassemia in Southeast Sicily. Am J Hematol 1995; 48:5-11. 9. Cao A, Gossens M, Pirastu M. -thalassaemia mutations in Mediterranean populations. Br J Haematol 1989; 71:309-12. 10. Vania A, Gentiloni Silverj F, Fruscella R, Plantamura M, Cianciulli P, Ballati G. Thalassemic syndromes in Latium: epidemiological evaluation. Haematologica 1998; 83:525-32.