1. Isodicentric chromosome 18 in an abnormal infant using chromosome specific DNA probe;Meguid, N.A.; Habibian, R.;Clin Genet,1992
2. Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocation;Pinkel, D.; Landegent, J.; Collins, C.,1988
3. A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres;Moyzis, R.K.; Buckingham, J.M.; Cram, L.S.,1988
4. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia;Saiki, R.K.; Scharf, S.; Faloona, F.;Science,1985
5. Tetranucleotide repeat polymorphism at the human myelin basic protein gene (MBP);Polymeropoulos, M.H.; Xiao, H.; Merril, C.R.;Hum Mol Genet,1992