The “diagnostic odyssey” – a unique and unpredictable journey towards hope
Orphanet Journal of Rare Diseases is proud to present this article by Chloe Yallop, a runner-up entry in beacon for rare diseases and… Read more »
Chloe Yallop is a final year Genetics student at The University of Manchester, with a particular interest into the study of (rare) genetic diseases. She hopes to pursue a career in Genetic Counselling and further contribute within the rare disease community, to raise awareness and improve the available support for affected individuals and their families.
Latest posts by Chloe Yallop (see all)
- The “diagnostic odyssey” – a unique and unpredictable journey towards hope - 26th February 2023