Literature DB >> 2319227

Highly polymorphic minisatellite sequences: allele frequencies and mutation rates for five locus-specific probes in a Caucasian population.

J C Smith1, R Anwar, J Riley, D Jenner, A F Markham, A J Jeffreys.   

Abstract

Six human minisatellite sequences (MS1, MS8, MS29, MS31, MS43, g3) have been subcloned into a stable host/vector system. Allele frequencies at the hypervariable loci detected by five of these probes were determined in a Caucasian population (200 individuals). Mendelian inheritance has been demonstrated in 5 large multi-generation pedigrees. The mutation rate has been determined in 59 families. The highest mutation rate was observed with MS1, as might be predicted from the observed high heterozygosity and in agreement with previous direct measurement of germ line mutation rates. The data presented on allele frequencies and mutation rates provide preliminary data supporting the use of these probes in paternity analysis and forensic investigations.

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Year:  1990        PMID: 2319227     DOI: 10.1016/s0015-7368(90)73298-7

Source DB:  PubMed          Journal:  J Forensic Sci Soc        ISSN: 0015-7368


  19 in total

1.  Haplotype fine mapping by evolutionary trees.

Authors:  J C Lam; K Roeder; B Devlin
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

Review 2.  Molecular biology in medicine.

Authors:  B D Young
Journal:  Postgrad Med J       Date:  1992-04       Impact factor: 2.401

3.  DNA investigations on fetal material from paternity cases.

Authors:  P Wiegand; J Lorente; B Brinkmann
Journal:  Int J Legal Med       Date:  1991       Impact factor: 2.686

4.  Population and family data of RFLP's using selected single- and multi-locus systems.

Authors:  B Brinkmann; S Rand; P Wiegand
Journal:  Int J Legal Med       Date:  1991-03       Impact factor: 2.686

5.  The distribution of the HLA-DQ alpha alleles and genotypes in the Finnish population as determined by the use of DNA amplification and allele specific oligonucleotides.

Authors:  A Sajantila; M Ström; B Budowle; P J Tienari; C Ehnholm; L Peltonen
Journal:  Int J Legal Med       Date:  1991       Impact factor: 2.686

6.  [Use of DNA polymorphism in forensic paternity evaluation].

Authors:  L Henke; H Paas; K Hoffmann; J Henke
Journal:  Z Rechtsmed       Date:  1990

7.  Recent observations in human DNA-minisatellite mutations.

Authors:  J Henke; L Henke
Journal:  Int J Legal Med       Date:  1995       Impact factor: 2.686

8.  Mutation rate in the hypervariable VNTR g3 (D7S22) is affected by allele length and a flanking DNA sequence polymorphism near the repeat array.

Authors:  R Andreassen; T Egeland; B Olaisen
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

9.  Population genetic and family data for the human minisatellite locus D16S309 (MS205) in Germans.

Authors:  L Henke; S Cleef; M Tahar; I Kops; J Henke
Journal:  Int J Legal Med       Date:  1996       Impact factor: 2.686

10.  Short alleles revealed by PCR demonstrate no heterozygote deficiency at minisatellite loci D1S7, D7S21, and D12S11.

Authors:  S Alonso; A Castro; I Fernández-Fernández; M M de Pancorbo
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

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