Literature DB >> 8547165

Observation of null alleles apparently due to deletions.

A Möller1, P Wiegand, B Brinkmann.   

Abstract

After examining 2 paternity cases in 17 classical, 4 RFLP and 5 PCR-VNTR systems, isolated pseudo-exclusions were observed in the polymorphism D2S44 (YNH24). In both cases the "exclusions" were due to apparent opposite homozygosity. The application of different restriction enzymes, PCR amplification and varying electrophoretic conditions each led to an equivalent result of a 1-band-pattern with a mismatch between both father/child pairs. From these results the authors conclude that a complete or almost complete loss of the alleles is the most probable explanation.

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Year:  1995        PMID: 8547165     DOI: 10.1007/bf01369911

Source DB:  PubMed          Journal:  Int J Legal Med        ISSN: 0937-9827            Impact factor:   2.686


  11 in total

1.  Population genetics and forensic efficiency data of 4 AMPFLP's.

Authors:  S Rand; C Puers; K Skowasch; P Wiegand; B Budowle; B Brinkmann
Journal:  Int J Legal Med       Date:  1992       Impact factor: 2.686

2.  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

3.  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

4.  Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

Authors:  A J Jeffreys; N J Royle; V Wilson; Z Wong
Journal:  Nature       Date:  1988-03-17       Impact factor: 49.962

5.  Population genetics of three VNTR polymorphisms in two different Spanish populations.

Authors:  E Valverde; C Cabrero; R Cao; M S Rodríguez-Calvo; A Díez; F Barros; J Alemany; A Carracedo
Journal:  Int J Legal Med       Date:  1993       Impact factor: 2.686

6.  Forensic validation of the STR systems SE 33 and TC 11.

Authors:  P Wiegand; B Budowle; S Rand; B Brinkmann
Journal:  Int J Legal Med       Date:  1993       Impact factor: 2.686

7.  Nondetectability of restriction fragments and independence of DNA fragment sizes within and between loci in RFLP typing of DNA.

Authors:  R Chakraborty; Y Zhong; L Jin; B Budowle
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

8.  DNA-minisatellite mutations: recent investigations concerning distribution and impact on parentage testing.

Authors:  J Henke; R Fimmers; M P Baur; L Henke
Journal:  Int J Legal Med       Date:  1993       Impact factor: 2.686

9.  PCR-amplification of D2S44 alleles.

Authors:  A Möller; C Puers; B Brinkmann
Journal:  Int J Legal Med       Date:  1994       Impact factor: 2.686

10.  Human population genetic studies of five hypervariable DNA loci.

Authors:  I Balazs; M Baird; M Clyne; E Meade
Journal:  Am J Hum Genet       Date:  1989-02       Impact factor: 11.025

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  2 in total

1.  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

2.  Retrospective selection of elite parent trees using paternity testing with microsatellite markers: an alternative short term breeding tactic for Eucalyptus.

Authors:  D Grattapaglia; V J Ribeiro; G D S P Rezende
Journal:  Theor Appl Genet       Date:  2004-03-05       Impact factor: 5.699

  2 in total

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