This module will provide an introduction to the clinical presentation and manifestations of rare inherited and common diseases, and considers the patient and family perspective with respect to the role and impact of genomics. It reviews traditional and current strategies and techniques used to identify genes responsible for both common multifactorial and rare inherited diseases.
FHEQ (what does this mean?)
Who should attend?
This course is ideal for those who wish to better understand the impact of genomics on the development of inherited diseases.
Presentation, Assignment 1
Swansea University Medical School,
Institute of Life Science 2,
How To Apply
For enquiries or to apply please contact Dr Claire Morgan.
Dr Anna Derrick