1. Buckle V. J., and Rack K. A. 1993. Fluorescent in situ hybridization. In K. E. Davis, ed., Human Genetic Disease Analysis: A Practical Approach (59–82). Oxford, UK: IRL Press at Oxford University Press.
2. Carter, N. P., Ferguson-Smith, M. A., Perryman, M. T., Telenius, H., Pelmear, A. H., Leversha, M. A., Glancy, M. T., Wood, S. L., Cook, K., Dyson, H. M., Ferguson-Smith, M. E., and Willat, L. R. 1992. Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics. Journal of Medical Genetics 29:299–307.
3. Delhanty, J. D. A., Harper, J. C., Ao, A., Handyside, A. H., and Winston, R. M. L. 1997. Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients. Human Genetics 99:755–760.
4. Devilee, P., Thierry R. F., and Kievits T. 1988. Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes. Cancer Research 48:5825–5830.
5. Gall J. G., and Pardue, M. L. 1969. Formation and detection of RNA-DNA hybrid molecules in cytological preparations. Proceedings of the National Academy of Sciences U.S.A. 63:378–383.