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2014 Annual Clinical Genetics Meeting
March 25, 2014 - March 29, 2014
162 Sessions, 11 Speakers
On Demand Recording

The 2014 Annual Clinical Genetics Meeting - sponsored by the American College of Medical Genetics and Genomics (ACMG) is available for purchase. The recordings consist of premiere leaders in the field of genetic and genomic medicine and provide genetics professionals with the opportunity to learn how genetics and genomics are being integrated into medical or clinical practice.

Every professional in the field of genetics and genomics will benefit from viewing the recordings. The meeting is targeted to medical and clinical geneticists, genetic counselors, pediatric, obstetric, maternal-fetal specialists and all medical practitioners who are providing comprehensive diagnostic, management and counseling services for patients with, or at risk for, genetically influenced health problems; laboratory directors and technicians conducting genetic testing; researchers involved in the discovery of genetic disorders and treatments; and all healthcare and public health professionals with an interest in medical and clinical genetics and genomics.

The session recordings do not include the ability to claim CME or CEU credit.
2014 ACMG Pre-Conference Workshop
7 Sessions
Transition to Evidence-based Clinical
Guidelines: Understanding Systematic
Review and Translation of Evidence to
2014 ACMG Short Course: A Neurogenetics Update
7 Sessions
A Neurogenetics Update
2014 ACMG Short Course: Labs are from Venus and Docs are from Mars
6 Sessions
Labs are from Venus and Docs are
from Mars:Interpretation and Reporting
of Sequence Variants
2014 Complete Online Library
140 Sessions
Includes unlimited online access to the 2014 ACMG meeting sessions. Does not include the pre-conference workshop or the short courses.

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Overview of the ACMG/AMP/CAP Interpretation of Sequence Variants Guideline
Using Public Databases and In Silico Tools as Resources for Variant Classification
The Zen of Variant Interpretation
Standardizing Reports and Structuring Results: Transitioning from Sanger to Next Generation Sequencing
How Should Physicians Integrate the New Variant Classification Guidelines into Clinical Care?