Résultat de recherche

Developmental cell death regulates lineage-related interneuron-oligodendroglia...

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...

PRA Instructions

Live 2

Mickaël Ménager

Nouvelle maladie génétique prédisposant aux mycobactéries : l’IFN-ɣ...

Inherited human IFN-γ deficiency underlies mycobacterial disease.

Un nouveau gène responsable d’anomalies du développement

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

Ttc7a, un frein de la prolifération de cellules souches

Comment se met en place la réponse immunitaire ?

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