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    • Spina Bifida & other Dysraphisms (WG13)
    • Fetal medicine and pathology (WG6)
    • Healthcare & CPMS (WG5)
    • Guidelines & consensus (WG11)
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    • APOGeE (WG9)
    • European Certificate (WG10)
    • Research & innovation (WG12)
    • Registries (WG7)
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    • ILIAD RD register
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    • Publications
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  • Guidelines
    • Methodology
    • ERN ITHACA Guidelines
    • Endorsed guidelines
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  • Education
    • Online Genetics Course APOGeE
    • Survival guide to genetics
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    • MOOC “bioinformatics”
    • Orphanet Updates
    • SysNDD Database
    • Training exchanges
    • Documentation for patients
  • News & Events
    • Webinars
    • EuroDysmorpho 2024
    • EuroNDD 2024
    • NSEuronet Meeting
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Home > Our Research Activities > List Of Publications > Germline AGO2 mutations impair RNA interference and human neurological development.

Germline AGO2 mutations impair RNA interference and human neurological development.

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Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndrome
10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in France.
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