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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Poulsen, L. Farzad, M. Sharafi Børsting, C. Tomas, C. Pereira, V. Morling, N. |
| Spatial Coverage | Iran |
| Description | Author Affiliation: Poulsen L ( Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Frederik V's Vej 11, DK-2100 Copenhagen, Denmark. Electronic address: lena.poulsen@sund.ku.dk.); Farzad MS ( Kawsar Human Genetics Research Center, 41 Majlesi St., Vali Asr St., Tehran, Iran.); Børsting C ( Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Frederik V's Vej 11, DK-2100 Copenhagen, Denmark.); Tomas C ( Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Frederik V's Vej 11, DK-2100 Copenhagen, Denmark.); Pereira V ( Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Frederik V's Vej 11, DK-2100 Copenhagen, Denmark.); Morling N ( Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Frederik V's Vej 11, DK-2100 Copenhagen, Denmark.) |
| Abstract | A total of 255 individuals (Persians, Lurs, Kurds and Azeris) from Iran were typed for three sets of forensic genetic markers with the NGM SElect™, DIPplex(®) and Argus X-12 kits. Statistically significant deviations (P≤0.002) from Hardy-Weinberg expectations were observed for the insertion-deletion markers HLD97 and HLD93 after Holm-Sidák correction. Statistically significant (P<0.05) levels of linkage disequilibrium were observed between markers within two of the four studied X-chromosomal linkage groups. AMOVA analyses of the three sets of markers did not show population structure when the individuals were grouped according to their ethnic group. The Iranian population grouped closely to populations living geographically near to Iran based on pairwise FST distances. The matching probabilities ranged from 1 in 3.2×10(7) males by using haplotype frequencies of four X-chromosomal haplogroups to 1 in 3.4×10(21) individuals for the 16 autosomal STRs. |
| File Format | HTM / HTML |
| ISSN | 18724973 |
| Volume Number | 17 |
| e-ISSN | 18780326 |
| Journal | Forensic Science International: Genetics |
| Language | English |
| Publisher | Elsevier |
| Publisher Date | 2015-07-01 |
| Publisher Place | Netherlands |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Discipline Forensic Sciences Ethnic Groups Genetics Forensic Genetics Methods Genetic Markers Indel Mutation Biological Markers Blood Dna Databases, Genetic Female Genetics, Population Genotype Haplotypes Humans Iran Male Microsatellite Repeats Journal Article |
| Content Type | Text |
| Resource Type | Article |
| Subject | Genetics Pathology and Forensic Medicine |
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