Résultat de recherche

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

How the study of genetic diseases contributes to knowledge in cancerol...

Diagnosing a common genetic mutation in multiple patients using unstructured...

Type 1 interferopathies: keys to understanding clinical and tissue var...

Marianna Parlato, a young researcher dedicated to inflammatory bowel d...

Rare epilepsies, where do we stand?

Science for children: The cell

Science for children: DNA

Science for children: Covid-19 and genetics

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

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

6 new rare disease reference centers affiliated to the Institut Imagin...

Erminia Rubino, business developer at Institut Imagine

Two type 1 interferopathies where the lung becomes inflamed

Understanding genetic deafness

Genetic deafness, which path of research and care for patients?

Genetic deafness: an update on these pathologies, research and care

Discover our web-conferences dedicated to rare diseases in replay

International Women's Day: They are looking for Imagine

Medetia : towards a first treatment of severe ciliopathy in children