Source:http://linkedlifedata.com/resource/pubmed/id/20492613
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2010-11-2
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pubmed:abstractText |
The analysis of X-chromosome markers can be valuable in particular situations, for example, deficiency kinship cases, where the putative father cannot be typed. X-chromosome short-tandem repeats (X-STRs) are widely used in forensic genetics, while the use of X-chromosome single-nucleotide polymorphisms (X-SNPs) is still limited.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1537-2995
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pubmed:author | |
pubmed:copyrightInfo |
© 2010 American Association of Blood Banks.
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pubmed:issnType |
Electronic
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pubmed:volume |
50
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2258-65
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pubmed:meshHeading |
pubmed-meshheading:20492613-Chromosomes, Human, X,
pubmed-meshheading:20492613-Female,
pubmed-meshheading:20492613-Haplotypes,
pubmed-meshheading:20492613-Humans,
pubmed-meshheading:20492613-Linkage Disequilibrium,
pubmed-meshheading:20492613-Male,
pubmed-meshheading:20492613-Microsatellite Repeats,
pubmed-meshheading:20492613-Mutation,
pubmed-meshheading:20492613-Polymorphism, Single Nucleotide
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pubmed:year |
2010
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pubmed:articleTitle |
Forensic usefulness of a 25 X-chromosome single-nucleotide polymorphism marker set.
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pubmed:affiliation |
Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark. carmen.tomas@forensic.ku.dk
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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