Manylion y Cwrs
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.
Lefel y Cwrs
FHEQ (beth yw ystyr hyn?)
Pwy ddylai fynychu
Mae'r cwrs hwn yn ddelfrydol ar gyfer y rhai sydd am ddeall yn well effaith genomeg ar ddatblygiad clefydau etifeddol.
Dyddiad
Tachwedd 2022
Hyd
Asesiad
Assignment 1, Assignment 2
Pris y Cwrs
£1,350.00
Lleoliad
Ysgol Feddygaeth Prifysgol Abertawe,
Institute of Life Science 2,
Swansea University,
Singleton Park,
Swansea,
SA2 8PP
Sut i Wneud Cais
Ar gyfer ymholidadau cysylltwch a Dr Claire Morgan.
Darlithwyr
Dr Anna Derrick