Fc-eRII/CD23 Receptor on Circulating Human Eosinophils

patients. Am J Hum Genet 30:828, 1997 7. Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJH: Global prevalence of putative haemochromatosis mutations. J Med Genet 34:275, 1997 8. Jazwinska EC, Cullen LM, Busfield F, Pyper WR, Webb SI, Powell LW, Morris CP, Walsh TP: Haemochromatosis and HLA-H. Nat Genet 14:249, 1996 (letter) 9. The UK Haemochromatosis Consortium: A simple genetic test identifies 90% of UK patients with haemochromatosis. Gut 41:841, 1997 10. Merryweather-Clarke AT, Liu Y-T, Shearman JD, Pointon JJ, Robson KJH: A rapid non-invasive method for the detection of the haemochromatosis C282Y mutation. Br J Haematol 99:460, 1997 11. Bowen DJ, Standen GR, Granville S, Bowley S, Wood NAP, Bidwell J: Genetic diagnosis of factor V Leiden using heteroduplex technology. Thromb Haemost 77:119, 1997 12. Rees DC, Cox M, Clegg JB: Detection of the factor V Leiden mutation using whole blood PCR. Thromb Haemost 75:520, 1995 (letter) 13. Jackson HA, Bowen DJ, Worwood M: Rapid genetic screening for haemochromatosis using heteroduplex technology. Br J Haematol 98:856, 1997 14. Smillie D: A PCR-SSP method for detecting the Cys282Tyr mutation in the HFE gene associated with hereditary haemochromatosis. J Clin Pathol–Mol Pathol 50:275, 1997 15. Bodmer J, Parham P, Albert ED, Marsh SGE: Putting a hold on ‘HLA-H’. Nat Genet 15:234, 1997 (letter)