Chromosome Analysis Using Spectral Karyotyping (SKY)

Cell Biochemistry and Biophysics

Volumn 62, Issue 1, 2012, Pages 13-17

  Imataka, George ^a   Arisaka, Osamu ^a  

^a DOKKYO MEDICAL UNIVERSITY   (Japan)

Author keywords

Chromosome SKY; Fluorescent in situ hybridization; Multicolor FISH; Spectral karyotyping

Indexed keywords

CHROMOSOME; CHROMOSOME 13; CHROMOSOME DELETION; CHROMOSOME DISORDER; GENETICS; HUMAN; REVIEW; SPECTRAL KARYOTYPING; TRISOMY;

CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES; CHROMOSOMES, HUMAN, PAIR 13; HUMANS; SPECTRAL KARYOTYPING; TRISOMY;

EID: 84855603339     PISSN: 10859195     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12013-011-9285-2     Document Type: Review

References (22)

1. Harper, P. S. (2006). The discovery of the human chromosome number in Lund, 1955-1956. Human Genetics, 119, 226-232.
2. Lejeune, J., Turpin, R., & Gautier, M. (1959). Mongolism; a chromosomal disease (trisomy). Bulletin de l'Academie Nationale de Medecine, 143, 256-265.
3. Imataka, G., Mitsui, M., Mitsui, N., Hirabayashi, H., Yamanouchi, H., et al. (2005). Down syndrome with acute epiglottitis. Pediatrics International, 47, 333-335.
4. Edwards, J. H., Harnden, D. G., Cameron, A. H., Crosse, V. M., & Wolff, O. H. (1960). A new trisomic syndrome. Lancet, 1, 787-790.
5. Imataka, G., Nitta, A., Suzumura, H., Watanabe, H., Yamanouchi, H., et al. (2007). Survival of trisomy 18 cases in Japan. Genetic Counseling, 18, 303-308.
6. Patau, K., Smith, D. W., Therman, E., Inhorn, S. L., & Wagner, H. P. (1960). Multiple congenital anomaly caused by an extra autosome. Lancet, 1, 790-793.
7. de Grouchy, J., Turleau, C., & Leonard, C. (1971). Study by fluorescence of a trisomy C mosaic, probably 8: 46, XY-47, XY,?8+. Annales de Genetique, 14, 69-72.
8. Iselius, L., Lindsten, J., Aurias, A., Fraccaro, M., Bastard, C., et al. (1983). The 11q; 22q translocation: A collaborative study of 20 new cases and analysis of 110 families. Human Genetics, 64, 343-355.
9. Imataka, G., Takaya, Y., Hagisawa, S., Yamanouchi, H., & Eguchi, M. (2004). Trisomy 11/22 diagnosed by spectral karyotyping (SKY). Genetic Counseling, 15, 391-394.
10. Ford, C. E., Jones, K. W., Polani, P. E., De Almeida, J. C., & Briggs, J. H. (1959). A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome). Lancet, 1, 711-713.
11. Tanner, J. M., Prader, A., Habich, H., & Ferguson-Smith, M. A. (1959). Genes on the Y chromosome influencing rate of maturation in man: Skeletal age studies in children with Klinefelter's (XXY) and Turner's (XO) syndromes. Lancet, 2, 141-144.
12. Yamanouchi, H., Imataka, G., Nakagawa, E., Nitta, A., Suzuki, N., et al. (2005). An analysis of epilepsy with chromosomal abnormalities. Brain and Development, 27, 370-377.
13. Moorhead, P. S., Nowell, P. C., Mellman, W. J., Battips, D. M., & Hungerford, D. A. (1960). Chromosome preparations of leukocytes cultured from human peripheral blood. Experimental Cell Research, 20, 613-616.
14. Nowell, P. C., & Hungerford, D. A. (1960). Chromosome studies on normal and leukemic human leukocytes. Journal of the National Cancer Institute, 25, 85-109.
15. Watson, J. D. (1990). The human genome project: Past, present, and future. Science, 248, 44-49.
16. Caspersson, T., Castleman, K. R., Lomakka, G., Modest, E. J., Moller, A., et al. (1971). Automatic karyotyping of quinacrine mustard stained human chromosomes. Experimental Cell Research, 67, 233-235.
17. Yunis, J. J., & Chandler, M. E. (1978). High-resolution chromosome analysis in clinical medicine. Progress in Clinical Pathology, 7, 267-288.
18. Trask, B. J. (1991). Fluorescence in situ hybridization: Applications in cytogenetics and gene mapping. Trends in Genetics, 7, 149-154.
19. Kallioniemi, A., Kallioniemi, O. P., Sudar, D., Rutovitz, D., Gray, J. W., et al. (1992). Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science, 258, 818-821.
20. Schrock, E., du Manoir, S., Veldman, T., Schoell, B., Wienberg, J., et al. (1996). Multicolor spectral karyotyping of human chromosomes. Science, 273, 494-497.
21. Allderdice, P. W., Davis, J. G., Miller, O. J., Klinger, H. P., Warburton, D., et al. (1969). The 13q-deletion syndrome. American Journal of Human Genetics, 21, 499-512.
22. Kakazu, N., Ashihara, E., Hada, S., Ueda, T., Sasaki, H., et al. (2001). Development of spectral colour banding in cytogenetic analysis. Lancet, 357, 529-530.