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1.
Int J Legal Med ; 121(5): 359-63, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17066276

RESUMEN

To estimate Y-chromosomal short tandem repeat (Y-STR) mutation rates, 15 loci (i.e., DYS19, DYS389 I/II, DYS390, and DYS393; DYS437, DYS438, DYS439, and DYS385; DYS391, DYS392, YCA II, and DXYS156) were analyzed in a sample of 1,029 father/son pairs from Westphalia, northwestern Germany. Among 15,435 meiotic allele transfers, 32 mutations were observed; thus, the mutation rate across all 15 Y-STR loci was 2.1 x 10(-3) per locus (95% C.I.: 1.5-3.0 x 10(-3)). With the exception of a three-repeat mutation at DYS385, all remaining mutations were single repeat mutations. Repeat losses were more frequent than gains (20:12), and the mutation rate appeared to increase with age. The Y haplogroups that were detected in the individuals showing a mutation reflect the haplogroup distribution in the Westphalian population. Additionally, the correlation of surnames and haplotypes was tested: Only 49 surnames occurred more than once, and only two men with the same rare surname shared the same haplotype. All other men with identical surnames carried different haplotypes.


Asunto(s)
Cromosomas Humanos Y , Genética de Población , Repeticiones de Microsatélite , Alelos , Alemania , Haplotipos , Humanos , Masculino , Mutación
2.
Forensic Sci Int Genet ; 1(3-4): 232-7, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-19083767

RESUMEN

The molecular origin of DNA mutations and the mutation rates were analyzed at 14 short tandem repeat (STR) loci with samples from trio cases derived from 10 different German population samples. STR loci comprised of D2S1360, D3S1744, D4S2366, D5S2500, D6S474, D7S1517, D8S1132, D10S2325, D12S391, D18S51, D19S246, D20S480, D21S226, and D22S689. In a total of 488 meioses, 16 isolated genetic inconsistencies in 8 different STRs were observed, whereas no mutations were found at the other loci. The data of five mutations suggested the presence of silent or null alleles due to sequence variation in primer binding site. This could be confirmed for four suspected cases by the use of alternative primer sets and by DNA sequence analyses. Furthermore, this study revealed nine new allelic variants at five different loci.


Asunto(s)
Genética de Población , Repeticiones de Microsatélite , Mutación , Alelos , Secuencia de Bases , ADN/genética , Cartilla de ADN/genética , Femenino , Genética Forense , Frecuencia de los Genes , Alemania , Humanos , Masculino
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