“The Affordable Care Act: Implications for Newborn Screening and Children with Genetic Conditions”

Meg Comeau, MHA

The Catalyst Center, Boston University


“Newborn Screening for Lysosomal Storage Disorders – A Comparative Effectiveness Study”

Dieter Matern, MD, PhD

The Mayo Clinic


“Clinical Whole Exome Sequencing: Outcomes and Indications for Testing”

Christine M. Eng, MD

Baylor College of Medicine


“Emerging Therapies for Glycogen Storage Disease”

Dwight D. Koeberl, MD, PhD

Duke University School of Medicine


“Advances in Non-Invasive Prenatal Testing”

Nicole Teed, MS, CGC

Medical Science Liaison, Sequenom, Inc.


“Developing a Genomic Medicine Program”

Bruce R. Korf, MD, PhD

University of Alabama at Birmingham


“Approach to the Diagnosis of Skeletal Dysplasia”

Michael B. Bober, MD, PhD

Thomas Jefferson Medical College

Alfred I. DuPont Hospital for Children


“Navigating Uncertainty and Unexpected Findings in Whole Genome Array Testing: A Discussion of Interpretation and Reporting Strategies”

Hutton M. Kearney, PhD, FACMG

Cytogenetics Laboratory, Mission Hospital