Identification of a D8S1179 primer binding site mutation and the validation of a primer designed to recover null alleles
- 1 May 2003
- journal article
- Published by Elsevier in Forensic Science International
- Vol. 133 (3) , 220-227
- https://doi.org/10.1016/s0379-0738(03)00035-5
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Developmental Validation of a Single-Tube Amplification of the 13 CODIS STR Loci, D2S1338, D19S433, and Amelogenin: The AmpFℓSTR® Identifiler® PCR Amplification KitJournal of Forensic Sciences, 2004
- Detection of a Primer-Binding Site Polymorphism for the STR Locus D16S539 Using the Powerplex® 1.1 System and Validation of a Degenerate Primer to Correct for the PolymorphismJournal of Forensic Sciences, 2002
- Constructing Universal Multiplex Pcr Systems for Comparative GenotypingJournal of Forensic Sciences, 2002
- STR primer concordance studyForensic Science International, 2001
- Non-amplification of an allele of the D8S1179 locus due to a point mutation.International journal of legal medicine, 2001
- Sequence variation in humans and other primates at six short tandem repeat loci used in forensic identity testingForensic Science International, 2001
- Concordance Study on Population Database Samples Using the PowerPlex™ 16 Kit and AmpFℓSTR® Profiler Plus™ Kit and AmpFℓSTR® COfiler™ KitJournal of Forensic Sciences, 2001
- Genetic variation at nine short tandem repeat loci in Chamorros and Filipinos from GuamLegal Medicine, 2000
- A highly discriminating octoplex short tandem repeat polymerase chain reaction system suitable for human individual identificationElectrophoresis, 1995
- A rapid chemiluminescent method for quanititation of human DNANucleic Acids Research, 1992