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About the course
This course provides a broad grounding in human genetics, with the emphasis on the molecular aspects of human genetics, particularly in relation to human disease.
It is aimed mainly at science graduates who seek research careers in areas such as fundamental human molecular genetics, genetic factors in human health and disease, or molecular and cytogenetic approaches to diagnosis.
The course is flexible, and updated regularly to reflect important advances in human genetics.
Teaching covers a wide range of topics, including the fundamentals of human genetics, clinical genetics and genomics, together with more advanced topics such as diabetes, cancer genetics, gene therapy, animal models and epigenetics.
Entry Requirements
Our minimum requirement is a 2.1 degree in biochemical sciences, genetics or another science-based degree.
Applicants who do not meet the academic requirements listed but who have substantial relevant industry experience may exceptionally be admitted following completion of a ‘Special Qualifying Exam’ (SQE)
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