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...

Complete hemispherotomy leads to lateralized functional organization and...

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

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

MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate...

Integrated care and research programs

MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hyp...

Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during...

Rare epilepsies, where do we stand?

Audrey Desgrange: Promoting Women in Science

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...

Volunteer

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

Erminia Rubino, business developer at Institut Imagine