Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Margurethe Stenersen"'
Publikováno v:
Human Mutation. 23:117-124
Precise estimates of mutation rates at Y-chromosomal microsatellite STR (short tandem repeat) loci make an important basis for paternity diagnostics and dating of Y chromosome lineage origins. There are indications of considerable locus mutation rate
Publikováno v:
Forensic Science International. 110:47-59
The paper extends on the traditional methodology used to quantify DNA evidence in paternity or identificationcases. By extending we imply that there are more than two alternatives to choose between. In a standard paternitycase the two competing expla
Publikováno v:
International Congress Series. 1288:374-376
Autosomal STR polymorphisms at 2 loci (D12S392 and D17S906) are presented. Samples from current paternity analysis ( n = 909) were analysed. The observed heterozygosities were 0.878 (D12S392) and 0.915 (D17S906). No significant deviation from Hardy
Identification by DNA analysis of the victims of the August 1996 Spitsbergen civil aircraft disaster
Publikováno v:
Nature Genetics. 15:402-405
Disaster victim identification traditionally relies on the combined efforts of police, dentists and pathologists, comparing ante mortem (AM) information from the missing persons with post mortem (PM) data from the dead bodies. In Western countries, d
Publikováno v:
International Congress Series. 1261:76-78
We have studied 1766 father–son pairs of confirmed paternity (a total of 15 894 meioses) in nine Y-STR loci. The fathers were also analysed in five biallelic markers defining haplogroups (Hg) 1, 2, 3, 4, 9 and 16. A total of 36 fragment length muta
Publikováno v:
International Congress Series. 1261:185-187
Autosomal STR polymorphisms at 15 loci and Y-chromosomal STR polymorphisms at 9 loci are presented. Samples from current immigration casework including individuals from Somalia ( n ∼100) and northern Iraq (Kurds) ( n ∼100) were analysed. For the
Publikováno v:
International Congress Series. 1261:316-318
Y-chromosomal polymorphisms at nine microsatellite and five biallelic markers in a Norwegian population sample are presented. In 1766 samples, 726 different lineages were encountered. Six known haplogroups were observed (Hg1, 2, 3, 4, 9 and 16). Locu
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 127(6)
Several haematological malignancies can be cured using allogeneic stem cell transplantation (SCT). Maximal tolerable chemoradiotherapy doses are given as part of the conditioning-regimen. This treatment causes substantial toxicity, and the procedure
Publikováno v:
Forensic science international. 164(1)
Y-chromosomal variation at five biallelic markers (Tat, YAP, 12f2, SRY 10831 and 92R7) and nine multiallelic short tandem repeat (STR) loci (DYS19, DYS389I, DYS389II, DYS390, DYS391, DYS392, DYS393, DYS385I/II and DYS388) in a Norwegian population sa
Publikováno v:
International Congress Series. 1288:372-373
Autosomal STR polymorphisms at 15 loci (D3S1358, THO1, D21S11, D18S51, Penta E, D5S818, D13S317, D7S820, D16S539, CSF1PO, Penta E, vWA, D8S1179, TPOX and FGA) are presented. Samples from current paternity analysis (n = 1380) were analysed. The observ