Course Details
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.
Course Level
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.
Date
November 2022
Duration
Assessment
Assignment 1, Assignment 2
Cost
£1,350.00
Location
Swansea University Medical School,
Institute of Life Science 2,
Swansea University,
Singleton Park,
Swansea,
SA2 8PP
How To Apply
For enquiries or to apply please contact Dr Claire Morgan.
Lecturer
Dr Anna Derrick