28.02.2013 Views

The Principles of Clinical Cytogenetics - Extra Materials - Springer

The Principles of Clinical Cytogenetics - Extra Materials - Springer

The Principles of Clinical Cytogenetics - Extra Materials - Springer

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Fluorescence In Situ Hybridization 489<br />

63. Taylor, C.P.F., Patel, K., Jones, T., Kiely, F., De Stavola, B.L., and Sheer, D. (1993) Diagnosis <strong>of</strong> Ewing’s sarcoma and<br />

peripheral neuroectomdermal tumour based on the detection <strong>of</strong> t(11;22) using fluorescence in situ hybridization. Br. J.<br />

Cancer 67, 128–133.<br />

64. Geurts van Kessel, A., dos Santos, N.R., Simons, A., et al. (1997) Molecular cytogenetics <strong>of</strong> bone and s<strong>of</strong>t tissue<br />

tumors. Cancer Genet. Cytogenet. 95, 67–73.<br />

65. Biegel, J.A., Nycum, L.M., Valentine, V., Barr, F.G., and Shapiro, D.N. (1995) Detection <strong>of</strong> the t(2;13)(q35;q14) and<br />

PAX3–FKHR fusion in alveolar rhabdomyosarcoma by fluorescence in situ hybridization. Genes, Chromosomes Cancer<br />

12, 186–192.<br />

66. Grady-Leopardi, E.F., Schwab, M., Ablin, A.R., and Rosenau, W. (1986) Detection <strong>of</strong> N-myc oncogene expression in<br />

human neuroblastoma by in situ hybridization and blot analysis: relationship to clinical outcome. Cancer Res. 46,<br />

3196–3199.<br />

67. Taylor, C.P., Bown, N.P., McGuckin, A.G., et al. (2000) Fluorescence in situ hybridization techniques for the rapid<br />

detection <strong>of</strong> genetic prognostic factors in neuroblastoma. United Kingdom’s cancer study group. Br. J. Cancer 83, 40–49.<br />

68. Press, M.F., Bernstein, L., Thomas, P.A., et al. (1997) HER-2/neu gene amplification characterized by fluorescence in<br />

situ hybridization: poor prognosis in node-negative breast carcinomas. J. Clin. Oncol. 15, 2894–2904.<br />

69. Xing, W.R., Gilchrist, K.W., Harris, C.P., Samson, W., and Meisner, L.F. (1996) FISH detection <strong>of</strong> HER-2/neu<br />

oncogene amplification in early onset breast cancer. Breast Cancer Res. Treat. 39, 203–121.<br />

70. Ross, J.S. and Fletcher, J.A. (1999) HER-2/neu (c-erb-B2) gene and protein in breast cancer. Am. J. Clin. Pathol.<br />

112(Suppl.), S53–S67.<br />

71. Messing, E.M. and Catalona, W.J. (1997) Urothelial tumors <strong>of</strong> the urinary tract. In Campbell’s Urology (Walsh, P.C.,<br />

Retic, A.B., Stamey, T.A., and Vaughan, E.D., eds.), WB Saunders, Philadelphia, pp. 2327–2382.<br />

72. Halling, K.C., King, W., Sokolova, I.A., Meyer, R.G., Burkhadt, H.M., and Halling, A.C., (2000) A comparison <strong>of</strong><br />

cytology and fluorescence in situ hybridization for the detection <strong>of</strong> urothelium carcinoma. J. Urol. 164, 1768–1775.<br />

73. Skacel, M., Fahmy, M., Brainard, J.A., et al. (2003) Multitarget fluorescence in situ hybridization assay detects transitional<br />

cell carcinoma in the majority <strong>of</strong> patients with bladder cancer and atypical or negative urine cytology. J. Urol.<br />

169, 2101–2105.<br />

74. Luke, S. and Shepelsky, M. (1998) FISH: recent advances and diagnostic aspects. Cell Vis. 5, 49–53.<br />

75. Levy, B., Dunn, T.M., Kaffe, S., Kardon, N., and Hirschhorn, K. (1998) <strong>Clinical</strong> applications <strong>of</strong> comparative genomic<br />

hybridization. Genet. Med. 1, 4–12.<br />

76. Snijders, A.M., Nowak, N., Segraves, R., et al. (2001) Assembly <strong>of</strong> microarays for genome-wide measurement <strong>of</strong> DNA<br />

copy number. Nature Genet. 29(3), 263–264.<br />

77. Pinkel, D., Segraves, R., Sudar, D., et al. (1998) High resolution analysis <strong>of</strong> DNA copy number variation using comparative<br />

genomic hybridization to microarrays. Nature Genet. 20, 207–211.<br />

78. Buckley, P.G., Mantripragada, K.K., Benetkiewicz, M., et al. (2002) A full-coverage, high-resolution human chromosome<br />

22 genomic microarray for clinical and research applications. Hum. Mol. Genet. 1, 3221–3229.<br />

79. Veltman, J.A., Schoenmakers, E.F., Eussen, B.H., et al. (2002) High-throughput analysis <strong>of</strong> subtelomeric chromosome<br />

rearrangements by use <strong>of</strong> array-based comparative genomic hybridization. Am. J. Hum. Genet. 70, 1269–1276.<br />

80. Pollack, J.R., Perou, C.M., Alizadeh, A.A., et al. (1999) Genome-wide analysis <strong>of</strong> DNA copy-number changes using<br />

cDNA microarrays. Nature Genet. 23, 41–46.<br />

81. Albertson, D.G., Ylstra, B., Segraves, R., et al. (2000) Quantitative mapping <strong>of</strong> amplicon structure by array CGH<br />

identifies CYP24 as a candidate oncogene. Nature Genet. 25, 144–146.<br />

82. Weiss, M.M., Snijders, A.M., Kuipers, E.J., et al. (2003) Determination <strong>of</strong> amplicon boundaries at 20q13.2 in tissue<br />

samples <strong>of</strong> human gastric adenocarcinomas by high-resolution microarray comparative genomic hybridization. J.<br />

Pathol. 200, 320–326.<br />

83. Veltman, J.A., Fridlyand, J., Pejavar, S., et al. (2003) Array-based comparative genomic hybridization for genomewide<br />

screening <strong>of</strong> DNA copy number in bladder tumors. Cancer Res. 1, 2872–2880.<br />

84. Heilstedt, H.A., Ballif, B.C., Howard, L.A., et al. (2003) Physical map <strong>of</strong> 1p36, placement <strong>of</strong> breakpoints in monosomy<br />

1p36, and clinical characterization <strong>of</strong> the syndrome. Am. J. Hum. Genet. 72, 1200–1212.<br />

85. Yu, W., Ballif, B.C., Kashork, C.D., et al. (2003) Development <strong>of</strong> a comparative genomic hybridization microarray and<br />

demonstration <strong>of</strong> its utility with 25 well-characterized 1p36 deletions. Hum. Mol. Genet. 12, 2145–2152.<br />

86. Schrock, E., du Manoir, S., Veldman, T., et al. (1996) Multicolor spectral karyotyping <strong>of</strong> human chromosomes. Science<br />

26, 494–497.<br />

87. Chudoba, I., Plesch, A., Lorch, T., Lemke, J., Claussen, U., and Senger, G. (1999) High resolution multicolor-banding:<br />

a new technique for refined FISH analysis <strong>of</strong> human chromosomes. Cytogenet. Cell Genet. 84, 156–160.<br />

88. Kraan, J., von Bergh, A.R., Kleiverda, K., et al. (2002) Multicolor Fiber FISH. Methods Mol. Biol. 204, 143–153.<br />

89. Wachtel, S.S. and Tharapel, A.T. (2002) FISH and PRINS: competing or complementary technologies? Am. J. Med.<br />

Genet. 107, 97–98.<br />

90. Carter, N.P. (1994) Cytogenetic analysis by chromosome painting. Cytometry 18, 2–10.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!