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• W2012337224 abstract "BioEssaysVolume 12, Issue 1 p. 44-46 Feature What's new: Genomic finger printing goes simple Diethard Tautz, Diethard Tautz Diethard Tautz is at the Institut für Genetik & Mikrobiologie der Universität München, Maria-Wardstr. 1a, 8000, München 19 (FRG)Search for more papers by this author Diethard Tautz, Diethard Tautz Diethard Tautz is at the Institut für Genetik & Mikrobiologie der Universität München, Maria-Wardstr. 1a, 8000, München 19 (FRG)Search for more papers by this author First published: January 1990 https://doi.org/10.1002/bies.950120111Citations: 10AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL References 1 Dover, G. A. (1980). Ignorant DNA? Nature 285, 618– 620. 2 Jeffreys, A. J., Wilson, V. and Thein, S. L. (1985). Hypervariable ‘minisatellite’ regions in human DNA. Nature 314, 67– 73. 3 Jeffreys, A. J., Wilson, V. and Thein, S. L. (1985). Individual specific ‘fingerprints’ of human DNA. Nature 316, 76– 79. 4 Nakumura, Y., Leppert, M., O'Conell, P., Wolff, R., Holm, T., Culver, M., Martin, C., Fujimoto, E., Hoff, M., Kumlin, E. and White, R. (1987). Variable number of tanden repeat (VNTR) markers for human gene mapping. Science 235, 1616– 1622. 5 Jeffreys, A. J., Royle, N. J., Wilson, V. and Wong, Z. (1988). Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA. Nature 332, 278– 281. 6 Ali, S., Müller, C. R. and Epplen, J. T. (1987). DNA finger printing by oligonucleotide probes specific for simple repeats. Hum. Genet. 74, 239– 243. 7 Lewin, R. (1989). Limits to DNA fingerprinting. Science 243, 1549– 1550. 8 Sakai, R. K., Gelfand, D. H., Stoffel, S., Scharf, S. J., Higuchi, R., Horn, G. T., Mullis, K. B. and Erlich, H. A. (1988). Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 239, 487– 491. 9 Tautz, D. and Renz, M. (1984). Simple sequences are ubiquitous repetitive components of eukaryotic genomes. Nucl. Acids Res. 12, 4127– 4138. 10 Levinson, G. and Gutman, G. A. (1987). Slipped-strand mispairing: a major mechanism for DNA sequence evolution. Mol. Biol. Evol. 4, 203– 221. 11 Morgan, A. R., Coulter, M. B., Flintoff, W. Y. and Paetkau, V. H. (1974). Enzymatic syntheses of deoxyribonucleic acids with repeating sequences. Biochemistry 13, 1596– 1603. 12 Tautz, D., Trick, M. and Dover, G. (1986). Cryptic simplicity in DNA is a major source of genetic variation. Nature 322, 652– 656. 13 Weber, J. L. and May, P. E. (1989). Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am. J. Hum. Genet. 44, 388– 396. 14 Litt, M. and Luty, J. A. (1989). A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene. Am. J. Hum. Genet. 44, 397– 401. 15 Tautz, D. (1989). Hypervariability of simple sequences as a general source for polymorphic DNA markers. Nucl. Acids Res. 17, 6463– 6471. 16 Smith, L. M., Sanders, J. Z., Kaiser, R. J., Hughes, P., Dodd, C., Connell, C. R., Heiner, C., Kent, S. B. H. and Hood, L. E. (1986). Fluorescence detection in automated DNA sequence analysis. Nature 321, 674– 679. Citing Literature Volume12, Issue1January 1990Pages 44-46 ReferencesRelatedInformation" @default.
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