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Expert Review of Molecular Diagnostics|April 19, 2005
Application of automation and information systems to forensic genetic specimen processingBenoît Leclair, Tom SchollJournal of Forensic Sciences|October 6, 2004
Enhanced kinship analysis and STR-based DNA typing for human identification in mass fatality incidents: the Swissair flight 111 disasterBenoît Leclair, Chantal J Frégeau, Kathy L Bowen, et al.Journal of Forensic Sciences|October 6, 2004
Systematic analysis of stutter percentages and allele peak height and peak area ratios at heterozygous STR loci for forensic casework and database samplesBenoît Leclair, Chantal J Frégeau, Kathy L Bowen, et al.Electrophoresis|March 9, 2004
Precision and accuracy in fluorescent short tandem repeat DNA typing: assessment of benefits imparted by the use of allelic ladders with the AmpF/STR Profiler Plus kitBenoît Leclair, Chantal J Frégeau, Kathy L Bowen, et al.Journal of Forensic Sciences|October 11, 2003
AmpFlSTR profiler Plus short tandem repeat DNA analysis of casework samples, mixture samples, and nonhuman DNA samples amplified under reduced PCR volume conditions (25 microL)Chantal J Frégeau, Kathy L Bowen, Benoît Leclair, et al.Journal of Forensic Sciences|October 11, 2003
STR DNA typing: increased sensitivity and efficient sample consumption using reduced PCR reaction volumesBenoît Leclair, Joanne B Sgueglia, Patricia C Wojtowicz, et al.The Journal of Molecular Diagnostics : JMD|February 1, 2005
A multi-exonic BRCA1 deletion identified in multiple families through single nucleotide polymorphism haplotype pair analysis and gene amplification with widely dispersed primer setsBenjamin D Ward, Brant C Hendrickson, Thaddeus Judkins, et al.Journal of Forensic Sciences|May 26, 2007
Bioinformatics and human identification in mass fatality incidents: the world trade center disasterBenoît Leclair, Robert Shaler, George R Carmody, et al.Cancer Research|November 4, 2005
Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutationsThaddeus Judkins, Brant C Hendrickson, Amie M Deffenbaugh, et al.Future Oncology (London, England)|August 17, 2018
Hereditary cancer testing challenges: assembling the analytical pieces to solve the patient clinical puzzleKarla R Bowles, Debora Mancini-DiNardo, Bradford Coffee, et al.Pageof 2