Multi step microsatellite mutations leading to mother-child double variance--a case of non-exclusion parentage.

  title={Multi step microsatellite mutations leading to mother-child double variance--a case of non-exclusion parentage.},
  author={Venkanna Narkuti and Ravi N Vellanki and Narasimha M. Oraganti and Lakshmi Narasu Mangamoori},
  journal={Clinica chimica acta; international journal of clinical chemistry},
  volume={411 13-14},

Tables from this paper

Maternal allele mutation: Slippage synthesis furnishing evolutionary trend
This case study indicates the extension of one microsatellite repeat motif (TATC) at locus D13S317 in the population of Rajasthan, which is a deviation from the Mendelian inheritance in paternal and maternal meiosis.
Analysis of genetic polymorphism of nine short tandem repeat loci in Chinese Han population of Henan province
The nine STR loci are highly polymorphic in Chinese Han population of Henan province and they may be of great value in forensic science and human population genetics.


Paternal exclusion: allele sharing in microsatellite testing
Investigations on inconclusive paternity due to atypical allele sharing in autosomal microsatellites were resolved with X- and Y-chromosome STR analyses confirming the case as non-paternity.
Mother-child double incompatibility at vWA and D5S818 loci in paternity testing
This is the first study of a maternally transmitted microsatellite mutation in the loci D5S818 and vWA in paternity DNA testing and convincingly established that the mother and suspected father are the biological parents of the questioned child.
Haplotype-assisted characterization of germline mutations at short tandem repeat loci
In this study, 98 families with 101 mutations were analyzed in depth in which a mutation had been observed at one of the four loci D3S1358, FGA, ACTBP2, and VWA and it was possible to identify the mutated structure and/or mutation event in the vast majority of cases.
Evaluation of the 124-plex SNP typing microarray for forensic testing.
Microsatellite null alleles in parentage analysis
Microsatellite null alleles in frequencies typically reported in the literature introduce rather inconsequential biases on average exclusion probabilities, but can introduce substantial errors into empirical assessments of specific mating events by leading to high frequencies of false parentage exclusions.
Genetic analysis of 18 X-linked short tandem repeat markers in Korean population.
ISFG: Recommendations on biostatistics in paternity testing.
Short tandem repeat typing technologies used in human identity testing.
A brief perspective on the technologies and issues involved in STR typing is offered.