Platform presentations of selected Genetics abstracts.
G02 - Copy Number Variant Analysis Improves the Diagnostic Yield in a Cohort of Pediatric Patients with
Previously Negative Constitutional Exome Sequencing Results
Elan Hahn, MD, University of Toronto, Toronto, Ontario, Canada
G11 - Mosaicism in Cancer Susceptibility Genes in Unselected Cancer Patients
Diana Mandelker, MD, PhD, Memorial Sloan Kettering Cancer Center, New York, NY, USA
G13 - Comparison of Universal versus Traditional Genetic Testing Models for Cancer Patients
Ozge Ceyhan-Birsoy, PhD, Memorial Sloan Kettering Cancer Center, New York, NY, USA
G23 - High-throughput Fetal-fraction Amplification Increases Analytical Performance of Noninvasive
Prenatal Screening
Dale Muzzey, PhD, Myriad Women's Health, Inc., South San Francisco, CA, USA
Objectives:
- Analyze platform presentations of abstracts highlighted by the Genetics Subdivision leadership as particularly significant.
- Evaluate the scientific merit and significance of these selected studies through further discussion with the authors.
Recording Date: November 17, 2020
Continuing Education Credit Information
CME/CMLE credit: 1.00 hr
Last day to purchase course and CE claim credit: February 16, 2024
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