Résultat de recherche

CRISPR/Cas9: a patch on the DNA double helix?

How the study of genetic diseases contributes to knowledge in cancerology

Diagnosing a common genetic mutation in multiple patients using unstructured health data

Type 1 interferopathies: keys to understanding clinical and tissue variations

Marianna Parlato, a young researcher dedicated to inflammatory bowel diseases

Integrated care and research programs

Rare epilepsies, where do we stand?

February 27 and 28, 2021: a weekend dedicated to rare diseases

From rare to frequent: the importance of conducting research on genetic diseases

6 new rare disease reference centers affiliated to the Institut Imagine

Two type 1 interferopathies where the lung becomes inflamed

Understanding genetic deafness