pubmed-article:9378129 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:9378129 | lifeskim:mentions | umls-concept:C0043381 | lld:lifeskim |
pubmed-article:9378129 | lifeskim:mentions | umls-concept:C0185125 | lld:lifeskim |
pubmed-article:9378129 | pubmed:issue | 9 | lld:pubmed |
pubmed-article:9378129 | pubmed:dateCreated | 1997-11-12 | lld:pubmed |
pubmed-article:9378129 | pubmed:abstractText | Y-chromosomal microsatellites have been investigated for the purposes of application to male identification, population genetics and population history. With nine markers, every male in a German population sample (n = 70) could be identified by an individual-specific Y microsatellite haplotype. The analysis of 474 unrelated males of nine human populations with seven markers revealed 301 different Y haplotypes. The analysis of molecular variance (AMOVA) approach was used to detect male population characteristics of Y microsatellite haplotypes. With pairwise comparisons of inter-population variance, most of the populations could be distinguished significantly. Sixty individuals from different male populations in Asia and Northern Europe carrying a novel Y-chromosomal T-->C transition show reduced microsatellite variability together with haplotype similarities. Microsatellite data suggest that the mutation occurred recently in Asia, supporting the hypothesis of Asian ancestry of some northern European populations. | lld:pubmed |
pubmed-article:9378129 | pubmed:language | eng | lld:pubmed |
pubmed-article:9378129 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9378129 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:9378129 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:9378129 | pubmed:month | Aug | lld:pubmed |
pubmed-article:9378129 | pubmed:issn | 0173-0835 | lld:pubmed |
pubmed-article:9378129 | pubmed:author | pubmed-author:NagyMM | lld:pubmed |
pubmed-article:9378129 | pubmed:author | pubmed-author:PandyaAA | lld:pubmed |
pubmed-article:9378129 | pubmed:author | pubmed-author:Tyler-SmithCC | lld:pubmed |
pubmed-article:9378129 | pubmed:author | pubmed-author:KrawczakMM | lld:pubmed |
pubmed-article:9378129 | pubmed:author | pubmed-author:de KnijffPP | lld:pubmed |
pubmed-article:9378129 | pubmed:author | pubmed-author:RoewerLL | lld:pubmed |
pubmed-article:9378129 | pubmed:author | pubmed-author:KayserMM | lld:pubmed |
pubmed-article:9378129 | pubmed:author | pubmed-author:DieltjesPP | lld:pubmed |
pubmed-article:9378129 | pubmed:author | pubmed-author:ZerjalTT | lld:pubmed |
pubmed-article:9378129 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:9378129 | pubmed:volume | 18 | lld:pubmed |
pubmed-article:9378129 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:9378129 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:9378129 | pubmed:pagination | 1602-7 | lld:pubmed |
pubmed-article:9378129 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:9378129 | pubmed:meshHeading | pubmed-meshheading:9378129-... | lld:pubmed |
pubmed-article:9378129 | pubmed:meshHeading | pubmed-meshheading:9378129-... | lld:pubmed |
pubmed-article:9378129 | pubmed:meshHeading | pubmed-meshheading:9378129-... | lld:pubmed |
pubmed-article:9378129 | pubmed:meshHeading | pubmed-meshheading:9378129-... | lld:pubmed |
pubmed-article:9378129 | pubmed:meshHeading | pubmed-meshheading:9378129-... | lld:pubmed |
pubmed-article:9378129 | pubmed:meshHeading | pubmed-meshheading:9378129-... | lld:pubmed |
pubmed-article:9378129 | pubmed:meshHeading | pubmed-meshheading:9378129-... | lld:pubmed |
pubmed-article:9378129 | pubmed:meshHeading | pubmed-meshheading:9378129-... | lld:pubmed |
pubmed-article:9378129 | pubmed:meshHeading | pubmed-meshheading:9378129-... | lld:pubmed |
pubmed-article:9378129 | pubmed:meshHeading | pubmed-meshheading:9378129-... | lld:pubmed |
pubmed-article:9378129 | pubmed:year | 1997 | lld:pubmed |
pubmed-article:9378129 | pubmed:articleTitle | Applications of microsatellite-based Y chromosome haplotyping. | lld:pubmed |
pubmed-article:9378129 | pubmed:affiliation | Institut für Gerichtliche Medizin, Humboldt-Universität zu Berlin, Germany. kayser@rz.charite.hu-berlin.de | lld:pubmed |
pubmed-article:9378129 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:9378129 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9378129 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9378129 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9378129 | lld:pubmed |