Researcher
Judith Melki
Persistent identifiers
References for this unit in public registries: they allow cross-checking with other sources and do not change when the name does.
Affiliation
Fields of expertise
malformation
Exome
Arthrogryposis Multiplex Congenita
vein of Galen
Scn1a
rare diseases
aneurysmal
molecular diagnosis
3 publications in HAL since 2022.
Data provenance
Sources : scanR, HAL. Data compiled on 27/10/2026. Found an error? It is corrected in the original source (HAL, RNSR, directory); see how.