References
- Thomas Caskey C, Edwards A, Hammond H A. DNA: the history and the future use in forensic analysis. Proceedings of the international symposium on the forensic aspects of DNA analysis, Quantico, Virginia. Government Printing Office, U.S. Washington, D.C., U.S. June, 19–23, 1989, FBI Academy
- Wyman A R., White R. A highly polymorphic locus in human DNA. Proc Natl Acad Sci USA 1980; 77: 6754–8
- Aho K, Leino U. Paternity and blood group evidence: Scandinavian practice. The International and Comparative Law Quaterly 1982; 31: 576–81
- Silver H. Paternity testing. Critical reviews in clinical laboratory sciences 1989; 27: 391–408, 0001
- Hardy G H. Mendelian proportions in mixed populations. Science 1908; 28: 49–50
- Weinberg W. Über den nachweis der vererbung beim menschen. Jahreshefte Ver. Vaterland. Naturkd. Wurttemburg, Stuttgart 1908; 64: 368–82
- Botstein D, White R, Skolnick M, Davis R. Construction of genetic linkage maps using restriction fragment length polymorphism. Am J Hum Genet 1980; 32: 314–31
- Mullis K B., Faloona F A. Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction. Methods in Enzymology, R Wu, Moldave K. Grossman. Academic Press, New York 1987; 155: 335–50
- Saiki R K., Scharf S, Faloona F, et al. Enzymatic amplification of β-globin genomic sequences and restriction site analysis for diagnosis of side cell anemia. Science 1985; 230: 1350–4
- Southern E M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 1975; 98: 503–17
- Jeffreys A J., Wilson V, Thein S L. Hypervariable “minisatellite regions in human DNA”. Nature 1985; 314: 67–73
- Jeffreys Wilson V., Thein S L. Individual-specific 'fingerprints' in human DNA. Nature 1985; 316: 76–9
- Jeffreys A J., Turner M, Depenham P. The efficiency of multilocus DNA fingerprint probes for individualization and establishment of family relationships, determined from extensive casework. Am J Hum Genet 1991; 48: 824–40
- Nakamura Y, Leppert M, O'Connell P, et al. Variable number of tandem repeat (VNTR) markers for human gene mapping. Science 1987; 235: 1616–22
- Budowle B, Giusti A M., Waye J S., et al. Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisons. Am J Hum Genet 1991; 48: 841–55
- Budowie B, Chakraborty R, Giusti A M., Eisenberg A J., Allen R. Analysis of the VNTR locus D1S80 by the PCR followed by high resolution PAGE. Am J Hum Genet 1991; 48: 137–44
- Sajantila A, Puomilahti S, Johnsson C, Ehnholm C. Amplification of reproducible allele markers for amplified fragment length polymorphism (Amp-FLP) analysis. Biotechniques, in press
- Sajantila A, Budowie B, Ström M, et al. Amplification of alleles at the D1S80 locus by the polymerase chain reaction: comparison of a Finnish and a North American population sample, and forensic case-work evaluation, submitted
- Helminen P, Sajantila A, Johnsson V, Lukka M, Ehnholm C, Peltonen L. Amplification (PCR) of three hypervariable regions in paternity determinations Molecular and Cellular Probes, in press
- Erlich H A., Bugawan T L. HLA class II gene polymorphism: DNA typing, evolution, and relationship to disease susceptibility. PCR technology–principles and applications for DNA amplification, H A. Erlich. Stockton Press, New York 1989; 193–208
- Comey C T., Budowle B. Validation studies of the analysis of the HLA-DQα locus using the polymerase chain reaction. J Forensic Sci, in press
- Nickerson D A., Kaiser R, Lappin S, Stewart J, Hood L, Landegren U. Automated DNA diagnostics using an ELISA-based oligonucleotide ligation assay. Proc Natl Acad Sci USA 1990; 87: 8923–7
- Syvänen A C., Aalto-Setälä K, Harju L, Kontula K, Söderlund H. A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E. Genomics 1990; 8: 684–92