- Mallory Zink
- BRENDA JOYCE
- Dottie WINGER
The Collaborative Genomics Conference is a monthly online case conference that provides laboratories across the country the opportunity to share unique and/or novel cases/case series with the aim of updating overall genetic knowledge, enhancing communication of genetic information across disciplines, and improving clinical laboratory practices for improved patient care.
PHD, MD, RN, Genetic counselors. Healthcare professionals who generate or use genomic/genetic data in their practice.
|Kimberly Anderson, M.S. CGC, Chair||Brenda Joyce, BA, Coordinator||Jesse Hunter, Ph.D|
|Dr. Stephen Meyn, MD, PhD||Fen Guo, MSc, Ph.D||Dottie Winger, MS|
|In support of improving patient care, the University of Wisconsin–Madison ICEP is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC) to provide continuing education for the healthcare team.|
Credit Designation Statements
American Medical Association (AMA)
The University of Wisconsin–Madison ICEP designates this live activity for a maximum of 1 AMA PRA Category 1 Credit™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Continuing Education Units
The University of Wisconsin–Madison ICEP, as a member of the University Professional & Continuing Education Association (UPCEA), authorizes this program for 0.1 continuing education units (CEUs) or 1 hour.
POLICY ON FACULTY AND SPONSOR DISCLOSURE
It is the policy of the University of Wisconsin–Madison ICEP, that the faculty, authors, planners, and other persons who may influence content of this CE activity disclose all relevant financial relationships with commercial interests in order to allow CE staff to identify and resolve any potential conflicts of interest. Faculty must also disclose any planned discussion of unlabeled/unapproved uses of drugs or devices during their presentation(s).
Detailed disclosures will be available prior to the start of the activity.
After participation in this RSS, participants will be able to:
- Recognize both common and rare genetic abnormalities associated with developmental delay, infertility, prenatal ultrasound findings, and oncology specimens.
- Demonstrate an improved ability to effectively communicate genetic information across healthcare team members from different professions and disciplines.