Résultat de recherche

Reallocation of Olfactory Cajal-Retzius Cells Shapes Neocortex Archite...

Recurrent RTTN mutation leading to severe microcephaly, polymicrogyria...

Mutations in TBR1 gene leads to cortical malformations and intellectual...

Further refinement of COL4A1 and COL4A2 related cortical malformations...

Homozygous NLRP1 gain-of-function mutation in siblings with a syndromic...

Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar...

Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic...

Heterogeneous clinical phenotypes and cerebral malformations reflected...

Mickaël Ménager

New genetic disease predisposing to mycobacteria: IFN-ɣ remains the s...

Inherited human IFN-γ deficiency underlies mycobacterial disease.

A new gene responsible for developmental abnormalities

Bi-allelic Variations of SMO in Humans Cause a Broad Spectrum of Developmental...

Ttc7a, a brake on stem cell proliferation

How does the immune response build up?

New Publication

Accelerate our research into genetic diseases

Donor Testimonial: André A.

Chronicle of a deconfinement

What are dispensable genes and which is their functional role in humans?...