Prenatal genetics

946 - Clinical Experience for Noninvasive Prenatal Screen in Assisted Reproductive Technology Pregnancies  

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938 - Incidental Findings Involving the Sex Chromosomes on cfDNA

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947 - The Sanford Health Preemptive Genetic Screening Program
949 - Screening Newborns with Genomic Sequencing Increases Short-Term Downstream Health Care Costs: Preliminary Findings from the BabySeq Project
952 - Implementation of a Hospital-Supported Clinical Undiagnosed Disease Program: 5 Years’ Experience
955 - Adaptation and Early Implementation of the PREMM5 Lynch Syndrome Risk Prediction Model in a Diverse Population 
956 - The Alabama Genomic Health Initiative
957 - Economic Burden of Infant-Onset (Type 1) Spinal Muscular Atrophy (SMA1): A Retrospective Claims Database Analysis
960 - Barriers to Insurance Authorization and Coordination of Medically Appropriate Genetic Testing: a Case for Insurance Goldcarding
962 - Preliminary Findings From an Ongoing Systematic Review of Processes and Outcomes Associated with Disclosure of ACMG 59 Secondary Findings
963 - From Recommendation to Implementation: Partnering with Insurers and Laboratories to Streamline Genetic Testing Workflow at a Multidisciplinary Developmental Medicine Clinic
967 - Comorbid Diagnoses, Medications, and Healthcare Provider Types Among Patients Diagnosed with Classical Homocystinuria