References

5. Gee S. (2001) Seeing the genome, part 2. Cytogenetics in colour—automated imaging systems for fluorescent in situ hybridization (FISH). GI.T. Imaging Microsc. 3, 4-7.

6. Brenner M. and Dunlay T. (n.d.) Fluorescence in situ hybridization: hardware and software implications in the research laboratory. Nikon Microscopy, www.microscopyu.com/articles/fluorescence/insitu/brennerinsitu.html (accessed May 22, 2003).

7. Speicher M.R., Gwyn Ballard S., and Ward D.C. (1996) Karyotyping human chromosomes by combinatorial multifluor FISH. Nature Genet. 12, 368-375.

8. Azofeifa J., Fauth C., Kraus J., et al. (2000) An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISH. Am. J. Hum. Genet. 66, 1684-1688.

9. Kirchoff M., Gerdes T., Maahr J., et al. (1999) Deletions below 10 megabasepairs are detected in comparative genomic hybridization by standard reference intervals. Genes Chromosomes Cancer 25, 410-413.

Clinical Cytogenetics

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