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pubmed-article:20492613pubmed:dateCreated2010-11-2lld:pubmed
pubmed-article:20492613pubmed:abstractTextThe 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.lld:pubmed
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pubmed-article:20492613pubmed:authorpubmed-author:TomasCarmenClld:pubmed
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pubmed-article:20492613pubmed:copyrightInfo© 2010 American Association of Blood Banks.lld:pubmed
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pubmed-article:20492613pubmed:volume50lld:pubmed
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pubmed-article:20492613pubmed:year2010lld:pubmed
pubmed-article:20492613pubmed:articleTitleForensic usefulness of a 25 X-chromosome single-nucleotide polymorphism marker set.lld:pubmed
pubmed-article:20492613pubmed:affiliationSection of Forensic Genetics, Department of Forensic Medicine, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark. carmen.tomas@forensic.ku.dklld:pubmed
pubmed-article:20492613pubmed:publicationTypeJournal Articlelld:pubmed
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