1. Detection of chromosome aberrations in the human interphase nucleus by vis"ualization of specific target DNAs with radioactive and nonradioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84;Cremer, T.; Landegent, J.; Bruckner, A.; Scholl, H.P.; Schardin, M.; Hager, H.D.,1986
2. Cytogenetic analysis using quantitative, high sensitivity, fluorescence hybridization;Pinkel, D.; Straume, T.; Gray, J.W.;Proc Nail Acad Sci USA,1986
3. Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes;Kuo, W.-L.; Tenjin, H.; Segraves, R.; Pinkel, D.; Golbus, M.S.; Gray, J.;Am J Hum Genet,1991
4. Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridization;Christensen, B.; BryndorfT, Philip; J, Lundsteen; C, Hansen; W.;Prenat Diagn,1992
5. Prenatal diagnosis with biotinylated chromosome specific probes;Guyot, B.; Bazin, A.; Sole, Y.; Julien, C.; Daffos, F.; Forestier, F.;Prenat Diagn,1988