References
- Smith D W. Autosomal abnormalities. Am J Obstet Gynecol 1964; 90: 1055–1077
- Young I D, Cook J P, Mehta L. Changing demography of trisomy 18. Arch Dis Child 1986; 61: 1035–1036
- Carter P E, Pearn J H, Bell J, Martin N, Anderson N G. Survival in trisomy 18. Clin Genet 1985; 27: 59–61
- David T J, Glew S. Morbidity of trisomy 18 includes delivery by caesearean section. Lancet 1980; 2: 1295
- Schneider A S, Mennuti M I, Zackai E H. High caeserean section in trisomy 18 births: A potential indication for late prenatal diagnosis. Am J Obstet Gynecol 1981; 140: 367–370
- Pinkel D, Straume T, Gray J W. Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc Natl Acad Sci USA 1986; 83: 2934–2938
- Peakman D C, Morton M F, Robinson A. Prenatal diagnosis techniques used to help in ruling out maternal cell contamination. J Med Genet 1977; 14: 37–39
- Yunis J J. High resolution of human chromosomes. Science 1976; 191: 1268–1270
- Seabright M. A rapid banding technique for human chromosomes. Lancet 1971; 2: 971–972
- Cremer T, Landegent J, Bruckner A. Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: Diagnosis of trisomy 18 with probe L1.84. Hum Genet 1986; 74: 346–352
- Johnson G D, de Nogueira Araujo GM C. A simple method of reducing the fading of immunofluorescence during microscopy. J Immun Methods 1981; 43: 349–3503
- Klinger K W, Landes G, Shook D. Rapid detection of chromosome aneuploidies in uncultured amniocytes using fluorescence in situ hybridization (FISH). Am J Hum Genet 1992; 51: 55–65