{{ (moduleVm.actions && moduleVm.changeStatus) ? moduleVm.status : '' }} Prenatal Diagnosis: Procedures and Genetic Testing Methods - Vol. 42, No. 15

Activity Steps


Method of Participation in the Learning Process/Evaluation Method

Successful completion of this activity includes reading the entire article and successfully completing the post-quiz and an evaluation form.

Getting the Most out of the Activity

As you prepare to participate in this activity, please reflect on your practice and your patients and identify clinical challenges you hope to have addressed.

While participating in the training, identify ways you can use newly acquired knowledge, strategies, and skills to enhance patient outcomes and your own professional development.

Learning Objectives

After completing this continuing education activity you will be able to:

  1. Distinguish among the various types of cytogenetic abnormalities, copy-number variants, and single-gene disorders in relation to prenatal diagnostic testing.
  2. Choose appropriate cytogenetic and molecular genetic tests for prenatal diagnosis.
  3. Outline patient counseling on the risks, benefits, and limitations of prenatal diagnostic tools and explain when to refer appropriately for genetic counseling.
Price: $49.00


  • ACCME 2.0 CME

Lippincott Continuing Medical Education Institute, Inc. is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.

Lippincott Continuing Medical Education Institute, Inc. designates this enduring material for a maximum of 2.0 AMA PRA Category 1 CreditsTM. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

Professions: Physician
Test Code: PGO1022
Published: October 31, 2022
Expires: 10/30/2024
Required Passing Score: 7/10 (70%)
Authors: Rose C. Mahoney, BS, Margaret M. Thorsen, MD, and Melissa Russo, MD
Categories: Gynecological , Obstetrical
Specialties: Gynecology, OB/GYN