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Case Reports in Genetics|March 22, 2016
False Negative Cell-Free DNA Screening Result in a Newborn with Trisomy 13Yang Cao, Nicole L Hoppman, Sarah E Kerr, et al.
Journal of Clinical Microbiology|May 15, 2015
Detection of Group A Streptococcus in Pharyngeal Swab Specimens by Use of the AmpliVue GAS Isothermal Helicase-Dependent Amplification AssayMatthew L Faron, Nathan A Ledeboer, Paul Granato, et al.
Electrophoresis|March 26, 2003
High-throughput analysis of telomerase by capillary electrophoresisDonald H Atha, Karen Miller, Anita D Sanow, et al.
Mayo Clinic Proceedings|March 14, 2007
Relationship between age-related macular degeneration-associated variants of complement factor H and LOC387715 with coronary artery diseaseJose S Pulido, Joseph P McConnell, Ryan J Lennon, et al.
Journal of Cancer Research and Clinical Oncology|November 18, 2005
MYH Y165C and G382D mutations in hepatocellular carcinoma and cholangiocarcinoma patientsLinnea M Baudhuin, Lewis R Roberts, Felicity T B Enders, et al.
Clinical Chemistry|October 21, 2006
Diagnosis of alpha-1-antitrypsin deficiency: An algorithm of quantification, genotyping, and phenotypingMelissa R Snyder, Jerry A Katzmann, Malinda L Butz, et al.
Journal of Proteome Research|March 22, 2014
Clinical proteome informatics workbench detects pathogenic mutations in hereditary amyloidosesSurendra Dasari, Jason D Theis, Julie A Vrana, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 1, 2012
Multisite validation study to determine performance characteristics of a 92-gene molecular cancer classifierSarah E Kerr, Catherine A Schnabel, Peggy S Sullivan, et al.
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