ACMG’s Genomics Annual Clinical Genetics Meeting showcases latest breakthroughs in genetics research

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Do you cover genetics, genomics, healthcare or medicine? The media are invited to register now for the American College of Medical Genetics and Genomics Annual Clinical Genetics Meeting, March 25-29, 2014 at the Nashville Convention Center.

From Incidental Findings to Whole Genome/Exome Sequencing to Cancer Genetics, the focus of the ACMG Meeting is on the actual practice of genetics and genomics in healthcare, showcasing the latest breakthroughs in genetics research and its practical applications to medical practice. The ACMG Annual Meeting attracts medical and scientific leaders from around the world working to apply research in the human genome to the diagnosis, management, treatment and prevention of genetic conditions and rare and common diseases.

Reporters will hear about the latest medical genetics research; have the opportunity to interact with doctors, laboratory professionals and genetic counselors about what is happening right now in genetics and genomics; and view the latest products available in the extensive exhibit hall.

Topics range from common conditions to rare diseases. Sessions include information of interest to the general public, to health professionals and to the industry/trade.

The ACMG Meeting is the genetics meeting most focused on the practical applications of genetic discoveries in the clinical setting. And the 2014 Meeting is already shattering records with a record number of abstracts submitted and attendee registration to date is at an all-time high.

Two Genetics Short Courses on Tuesday, March 25:

  • Labs are from Venus and Docs are from Mars: Interpretation and Reporting of Sequence Variants
  • A Neurogenetics Update

 

Program Highlights:

  • Point/Counterpoint: One Year Later - The ACMG Recommendations for Reporting of Incidental Findings
  • "Duty to Recontact" in the Genomics Era
  • Access Issues in Genetics & the Affordable Care Act
  • Clinical Sequencing: What Have We Learned
  • Standing at the Crossroads: The Intersection of Pediatric Oncology and Clinical Genetics
  • Recent Advances in Neonatal Genetics
  • Telegenetics and Expanding Access to Genetic Services
  • Building Shared Genomic Resources
  • Noninvasive Prenatal Testing
  • Transition to Evidence-based Clinical Guidelines

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