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Abstract

The formal genetics of the PGM1 system has been questioned due to unexplained maternity exclusions and single paternity exclusions (Wetterling 1986, 1988; Bertrams 1988).

Keywords

Paternity Testing PGM1 Locus Paternity Investigation Single Paternity Phenotype 1A2B 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. Bertrams J, Weber W, Hoher PG (1988) On the significance of isolated exclusions in the PGM1 subtype system. In: Mayr WR (eds) Advances in Forensic Haemogenetics 2. Springer, Berlin Heidelberg, p 102Google Scholar
  2. Carter ND, West CM, Ernes E, Parkin B, Marshall WH (1979) Phosphoglucomutase polymorphism detected by isoelectric focusing: gene frequencies, evolution and linkage. Ann Hum Biol 6: 221–230PubMedCrossRefGoogle Scholar
  3. Takahashi N, Neel J, Satoh C, Nishizaki J, Masunari N (1982) A phylogeny for the principal alleles of the human phosphoglu- comutase-1 locus. Proc Nat Acad Sci, USA 79: 6636–6640CrossRefGoogle Scholar
  4. Wetterling G (1986) Incompatible mother-child pairs found in the PGM1 system. In: Brinkmann B, Henningsen K (eds) Advances in Forensic haemogentics 1. Springer, Berlin Heidelberg, p 186Google Scholar
  5. Wetterling G (1988) Discrepancy between gene and protein products within the PGM1 system shown by improved resolution on immobiline gels. In: Mayr WR (eds) Advances in forensic Haemogenetics 2. Springer, Berlin Heidelberg, p 97Google Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 1990

Authors and Affiliations

  • G. Wetterling
    • 1
  1. 1.State Institute for Blood Group SerologyUniversity HospitalLinköpingSweden

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