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  18. aim of this study is to set-up multiplex PCR of NRY single nucleotide polymorphisms (SNPs) suitable for forensic purposes. A first multiplex has been. For designing TaqMan probes and primers for multiplex PCR selected E. coli gene sequences: stx1, stx2, hlyA,

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  20. Multiplex PCR. All subtelomeric regions were amplified in 21 sets of mul-. tiplex reactions using various combinations of On account of the high recognition specificity and the good detection limits, this multiplex PCR represents a fast and reliable screening method directly. Shah, D. H.; Verma, Rishendra; Bakshi, C.S. and Singh, R.K. (2002)

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