Showing results (41-50 of 83) with videos related to
Sort By:
Pageof 9
American Journal of Clinical Pathology|August 1, 1989
Plasma cell malignancy in the acquired immune deficiency syndrome. Association with Epstein-Barr virusK V Voelkerding, L M Sandhaus, H C Kim, et al.Journal of Biomolecular Techniques : JBT|September 3, 2010
Multi-sample pooling and illumina genome analyzer sequencing methods to determine gene sequence variation for database developmentRebecca L Margraf, Jacob D Durtschi, Shale Dames, et al.Archives of Pathology & Laboratory Medicine|July 9, 2016
A Model Study of In Silico Proficiency Testing for Clinical Next-Generation SequencingEric J Duncavage, Haley J Abel, Jason D Merker, et al.American Journal of Clinical Pathology|July 1, 1996
Factor V R506Q gene mutation analysis by PCR-RFLP: optimization, comparison with functional testing for resistance to activated protein C, and establishment of cell line controlsK V Voelkerding, L Wu, E C Williams, et al.The Journal of Molecular Diagnostics : JMD|August 13, 2021
Creation of an Expert Curated Variant List for Clinical Genomic Test Development and Validation: A ClinGen and GeT-RM Collaborative ProjectEmma Wilcox, Steven M Harrison, Edward Lockhart, et al.Journal of Medical Microbiology|August 11, 2005
Increased sensitivity of bacterial detection in cerebrospinal fluid by fluorescent staining on low-fluorescence membrane filtersJacob D Durtschi, Maria Erali, L Kathryn Bromley, et al.Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|March 21, 2001
Analysis of the factor V Leiden mutation using the READIT AssayR B Rhodes, K Lewis, J Shultz, et al.Journal of Clinical Bioinformatics|January 25, 2013
Cystic fibrosis testing in a referral laboratory: results and lessons from a six-year periodPerry G Ridge, Christine Miller, Pinar Bayrak-Toydemir, et al.Archives of Pathology & Laboratory Medicine|March 22, 2017
Development and Validation of Targeted Next-Generation Sequencing Panels for Detection of Germline Variants in Inherited DiseasesAvni Santani, Jill Murrell, Birgit Funke, et al.The Journal of Molecular Diagnostics : JMD|January 4, 2019
Designing and Implementing NGS Tests for Inherited Disorders: A Practical Framework with Step-by-Step Guidance for Clinical LaboratoriesAvni Santani, Birgitte B Simen, Marian Briggs, et al.Pageof 9