1. Adams, P. C., A. E. Kertesz and L. S. Valberg, 1991. Clinical presentation of hemochromatosis: a changing scene. Am. J. Med. 90: 445–449.
2. Adams, P. C., M. Speechley and A. E. Kertesz, 1991. Long-term survival analysis in hereditary hemochromatosis. Gastroenterology 101: 368–372.
3. Aslanidis, C., G. Jansen, C. Amemiya, G. Shutter, M. Mahadevan, C. Tsilfidis, C. Chen, J. Alleman, N. G. M. Wormskamp, M. Vooijs, J. Buxton, K. Johnson, H. J. M. Smeets, G. G. Lennon, A. V. Carrano, R. G. Korneluk, B. Wieringa and P. J. de Jong, 1992. Cloning of the essential myotonic dystrophy region and mapping of putative defect. Nature 355: 548–551.
4. Borecki, I. B., G. M. Lathrop, G. E. Bonney, J. Yaouang and D. C. Rao, 1990. Combined segregation and linkage analysis of genetic hemochromatosis using affection status, serum iron, and HLA. Am. J. Hum. Genet. 47: 542–550.
5. Bothwell, T. H., R. W. Charlton and A. G. Motulsky, 1983. Hemochromatosis, pp. 1269–1298 in The Metabolic Basis of Inherited Disease, edited by J. B. Stanbury, J. B. Wyngaarden, D. S. Frederickson, J. L. Goldstein and M. S. Brown. McGraw-Hill, New York.