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Robert D Daber

Showing results (1-10 of 15) with videos related to

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Journal of Pathology Informatics|September 25, 2014
Development and implementation of a custom integrated database with dashboards to assist with hematopathology specimen triage and trafficElizabeth M Azzato, Jennifer J D Morrissette, Regina D Halbiger, et al.
Cancer Genetics|September 3, 2014
What you are missing could matter: a rare, complex BRAF mutation affecting codons 599, 600, and 601 uncovered by next generation sequencingMelissa A Wilson, Jennifer J D Morrissette, Suzanne McGettigan, et al.
Cancer Genetics|January 31, 2012
Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemiaLinsheng Zhang, Iya Znoyko, Luciano J Costa, et al.
European Journal of Medical Genetics|March 13, 2012
Ring chromosome 20Robert D Daber, Laura K Conlin, Laura D Leonard, et al.
Plos One|April 5, 2016
Building a Robust Tumor Profiling Program: Synergy between Next-Generation Sequencing and Targeted Single-Gene TestingMatthew C Hiemenz, Stephan Kadauke, David B Lieberman, et al.
Frontiers in Immunology|February 14, 2014
Trials and Tribulations with VH ReplacementWenzhao Meng, Sahana Jayaraman, Bochao Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 8, 2026
Diagnostic Yield of Exome Reanalysis Over Time: Contribution of Reevaluation Type, Timing, and Patient PhenotypeYi-Lee Ting, Trevor J Williams, Hillery Metz, et al.
Plos One|April 7, 2016
A Modified Integrated Genetic Model for Risk Prediction in Younger Patients with Acute Myeloid LeukemiaCaroline E Sloan, Marlise R Luskin, Anne M Boccuti, et al.
Cancer Genetics|December 17, 2018
Validation of a next-generation sequencing oncology panel optimized for low input DNARobyn T Sussman, Sydney Shaffer, Elizabeth M Azzato, et al.
Leukemia Research|January 9, 2018
Genotypic and clinical heterogeneity within NCCN favorable-risk acute myeloid leukemiaStephen A Strickland, Aaron C Shaver, Michael Byrne, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Pathology Informatics|September 25, 2014
Development and implementation of a custom integrated database with dashboards to assist with hematopathology specimen triage and trafficElizabeth M Azzato, Jennifer J D Morrissette, Regina D Halbiger, et al.
Cancer Genetics|September 3, 2014
What you are missing could matter: a rare, complex BRAF mutation affecting codons 599, 600, and 601 uncovered by next generation sequencingMelissa A Wilson, Jennifer J D Morrissette, Suzanne McGettigan, et al.
Cancer Genetics|January 31, 2012
Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemiaLinsheng Zhang, Iya Znoyko, Luciano J Costa, et al.
European Journal of Medical Genetics|March 13, 2012
Ring chromosome 20Robert D Daber, Laura K Conlin, Laura D Leonard, et al.
Plos One|April 5, 2016
Building a Robust Tumor Profiling Program: Synergy between Next-Generation Sequencing and Targeted Single-Gene TestingMatthew C Hiemenz, Stephan Kadauke, David B Lieberman, et al.
Frontiers in Immunology|February 14, 2014
Trials and Tribulations with VH ReplacementWenzhao Meng, Sahana Jayaraman, Bochao Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 8, 2026
Diagnostic Yield of Exome Reanalysis Over Time: Contribution of Reevaluation Type, Timing, and Patient PhenotypeYi-Lee Ting, Trevor J Williams, Hillery Metz, et al.
Plos One|April 7, 2016
A Modified Integrated Genetic Model for Risk Prediction in Younger Patients with Acute Myeloid LeukemiaCaroline E Sloan, Marlise R Luskin, Anne M Boccuti, et al.
Cancer Genetics|December 17, 2018
Validation of a next-generation sequencing oncology panel optimized for low input DNARobyn T Sussman, Sydney Shaffer, Elizabeth M Azzato, et al.
Leukemia Research|January 9, 2018
Genotypic and clinical heterogeneity within NCCN favorable-risk acute myeloid leukemiaStephen A Strickland, Aaron C Shaver, Michael Byrne, et al.
Pageof 2