Distinguishing minisatellite mutation from non-paternity by MVR-PCR.
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[1] A. Jeffreys,et al. Digital DNA typing at a second hypervariable locus by minisatellite variant repeat mapping. , 1993, Human molecular genetics.
[2] A. Jeffreys,et al. Minisatellite repeat coding as a digital approach to DNA typing , 1991, Nature.
[3] A. Jeffreys,et al. Complex gene conversion events in germline mutation at human minisatellites , 1994, Nature Genetics.
[4] R. Uchihi,et al. Applications of minisatellite variant repeat (MVR) mapping for maternal identification from remains of an infant and placenta. , 1995, Journal of forensic sciences.
[5] A. Jeffreys,et al. DNA typing of the D1S8 (MS32) locus by rapid detection minisatellite variant repeat (MVR) mapping using polymerase chain reaction (PCR) assay. , 1994, Forensic science international.
[6] G Vergnaud,et al. Complex recombination events at the hypermutable minisatellite CEB1 (D2S90). , 1994, The EMBO journal.
[7] A. Jeffreys,et al. Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism , 1994, Nature Genetics.
[8] A J Jeffreys,et al. Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability. , 1993, Human molecular genetics.
[9] Swee Lay Thein,et al. Hypervariable ‘minisatellite’ regions in human DNA , 1985, Nature.
[10] A. Jeffreys,et al. The use of minisatellite variant repeat-polymerase chain reaction (MVR-PCR) to determine the source of saliva on a used postage stamp. , 1994, Journal of forensic sciences.
[11] A. Jeffreys,et al. Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA , 1988, Nature.
[12] D. Klarkowski,et al. DNA analysis in disputed parentage: The occurrence of two apparently false exclusions of paternity, both at short tandem repeat (STR) loci, in the one child , 1997, Electrophoresis.
[13] A J Jeffreys,et al. The potential contribution of MVR-PCR to paternity probabilities in a case lacking a mother. , 1999, Journal of forensic sciences.
[14] A. Jeffreys,et al. Human minisatellites, repeat DNA instability and meiotic recombination , 1999, Electrophoresis.
[15] R. Uchihi,et al. Potential forensic applications of minisatellite variant repeat (MVR) mapping using the polymerase chain reaction (PCR) at D1S8. , 1994, Journal of forensic sciences.
[16] R. Chakraborty,et al. Paternity exclusion by DNA markers: effects of paternal mutations. , 1996, Journal of forensic sciences.
[17] Y E Dubrova,et al. Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7. , 1999, Human molecular genetics.