26 March 2018 - Wellcome Genome Campus, Hinxton, Cambridge
26-28 March 2018
This event explores how cutting-edge genomic research translates into clinical care and informs our understanding of the biology of rare disease.
The conference features the latest findings related to the genomic basis of rare diseases, providing insights into human biology, disease mechanisms and therapeutic approaches and provides a multi-disciplinary forum for clinicians (consultants and trainees), research and clinical scientists and bio-informaticians interested in understanding the impact of recent advances in genomics and technology on the care of patients with rare diseases.
For further information on speakers, registration and abstracts (deadline 30 January), click here.