1. Bearn, A. G. (1966). Wilson's disease. In Stanbury, J. B., Wyngaarden, J. B., and Frederickson, D. S. (eds.), The Molecular Basis of Inherited Diseases, 2nd ed., McGraw-Hill, New York, pp. 761?779.
2. Broman, L. (1964). Chromatographic and magnetic studies on human ceruloplasmin. Acta Soc. Med. Upsal. 69: Suppl. 7.
3. Cox, D. W., Fraser, F. C., and Sass-Kortsak, A. (1972). A genetic study of Wilson's disease: Evidence for heterogeneity. Am. J. Hum. Genet. 24646.
4. Delovitch, T., Davis, B., Holme, G., and Sehon, A. (1972). Isolation of messenger-like RNA molecules from immunochemically separated polyribosomes. J. Mol. Biol. 69373.
5. Housman, D., Forget, B., Skoultchi, A., and Benz, E. (1973). Quantitative deficiency of chain-specific globin messenger ribonucleic acid in the thalassemia syndromes. Proc. Natl. Acad. Sci. 701809.