Raresummit23 Testimonial From Kate Downes, East Genomics Laboratory Hub

RAREsummit23 Testimonial from Kate Downes, East Genomics Laboratory Hub

Cambridge Rare Disease Network (CamRARE)

RAREsummit23 Testimonial from Suzanne Drury, Congenica

Cambridge Rare Disease Network (CamRARE)

RAREsummit23: Testimonial from Joanna Davidge, LifeArc

Cambridge Rare Disease Network (CamRARE)

Genomics Conversation week 2023: 'Clinicians' Stories' - Kate Downes, Familial Hypercholesteraemia

Rare Disease Day 2024 - overview with Lucy McKay, Medics4RareDiseases

CRDN RAREsummit19 Testimonial by Genomic Laboratory Hub, CUH, Addenbrookes

Cambridge Rare Disease Network (CamRARE)

RAREsummit23 Testimonial from Siddarth Banka

Cambridge Rare Disease Network (CamRARE)

Rare Disease Day 2023

An introduction to Rare Disease (Genomics Conversation Week 2023)

Rare Disease Day 2022: Dr. Caroline Kuo

David Geffen School of Medicine at UCLA

CDKL5 | Rare Disease Day 2024

International Foundation for CDKL5 Research

Generation Genome - CRDN's RAREsummit21

Cambridge Rare Disease Network (CamRARE)

Scientist Stories: Heidi Rehm, Clinical Genomics

Katie Tate, Bioinformatics Analyst at Congenica, talks about rare disease for Rare Disease Day 2022

Rare Research and Funding

Cambridge Rare Disease Network (CamRARE)

Genomics of Rare Diseases 2023 | Keynote by Cynthia Morton, University of Manchester, UK

Wellcome Connecting Science Learning and Training