Single and double incompatibility at vWA and D8S1179/D21S11 loci between mother and child: implications in kinship analysis.

@article{Narkuti2008SingleAD,
  title={Single and double incompatibility at vWA and D8S1179/D21S11 loci between mother and child: implications in kinship analysis.},
  author={Venkanna Narkuti and Ravi N Vellanki and Naveen Anubrolu and Kiran Kumar Doddapaneni and Purna Chandra Gandhi Kaza and Lakshmi Narasu Mangamoori},
  journal={Clinica chimica acta; international journal of clinical chemistry},
  year={2008},
  volume={395 1-2},
  pages={
          162-5
        }
}

Figures and Tables from this paper

De novo deletion at D13S317 locus: a case of paternal-child allele mismatch identified by microsatellite typing.
Haplotype-assisted characterization of germline mutations at short tandem repeat loci
TLDR
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.
Multi step microsatellite mutations leading to mother-child double variance--a case of non-exclusion parentage.
Risk analysis of duo parentage testing with limited STR loci.
TLDR
Whether the Goldeneye 20A system (containing 19 short tandem repeats) can avert the shortage of duo parentage tests is evaluated and the mutation and exclusion rates detected accorded with the corresponding rates identified in the Identifiler system.
Mutations of short tandem repeat loci in cases of paternity testing in Chinese
TLDR
Among 15 STR loci, the highest mutation rate was observed in D12S391, but the D5S818 gene mutations rate was relatively low, and the mutations in this study mainly showed paternal mutation.
Analysis of an "off-ladder" allele at the Penta D short tandem repeat locus.
TLDR
Improved the range of DNA data available for this locus and enhanced the ability for individual identification of gene loci in this study.
SIBLING PAIR ANALYSIS IN THE IDENTIFICATION PROCESS OF THE MADURESE POPULATION USING STR CODIS LOCI
TLDR
The findings proved that the male-male siblings of the Madurese population had the highest allele sharing percentage at the loci of D13S317, D16S539, and D21S11.
...
...

References

SHOWING 1-10 OF 15 REFERENCES
Mother-child double incompatibility at vWA and D5S818 loci in paternity testing
TLDR
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.
Microsatellite mutation in the maternally/paternally transmitted D18S51 locus: two cases of allele mismatch in the child.
Multistep microsatellite mutation in the maternally transmitted locus D13S317: a case of maternal allele mismatch in the child
TLDR
The sequence of two hypervariable regions of mitochondrial DNA, HV1 and HV2 and the maternal alleles of six X chromosome STR loci in the questioned child matched completely with the mother.
Mutation in the STR locus D21S1 1 of father causing allele mismatch in the child.
TLDR
A case of paternity dispute with 15 autosomal STR loci and found a mismatch in one of the alleles of the locus D21S11 in the child suggests that the suspicious father is the biological father of the child.
Complex mutational events at the HumD21S11 locus
TLDR
The Ovambos and Papuans showed a better fit to the infinite allele model than to the stepwise mutation model, and in the German, Japanese and Chinese populations no significant bias towards one of the two models could be observed.
Genetic analysis of 18 X-linked short tandem repeat markers in Korean population.
“Paterniplex”, a highly discriminative decaplex STR multiplex tailored for investigating special problems in paternity testing
TLDR
A STR multiplex suitable for solving complex paternity cases such as deficiency cases or cases with mutations, and three examples for cases that could not be solved using commercially available kits alone, but using the Paterniplex in addition to a commercial kit.
Y‐chromosome and mitochondrial DNA polymorphisms in Indian populations
Y‐chromosome polymorphism using short tandem repeat (STR) markers on 94 normal males belonging to the Brahmin and Kamma caste populations of Andhra Pradesh, India, and Siddis, a migrant population
...
...