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  3. Avis 8912 - NIPT

Avis 8912 - NIPT

07/05/2014
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Mise en œuvre du screening génétique prénatal non invasif de la trisomie 21 (Syndrome de Down) dans la pratique des soins de santé en Belgique (mai 2014) (CSS 8912)

  • Advise 8912 - NIPT

    English
    Implementation of non-invasive prenatal genetic screening for trisomy 21 (Down Syndrome) in the practice of health care in Belgium (May 2014) (SHC 8912).pdf PDF document - 870.98 KB
  • Advies 8912 - NIPT

    Dutch
    Implementatie van niet-invasieve prenatale genetische screening van trisomie 21 (Syndroom van Down) in de Belgische zorgpraktijk (mei 2014) (HGR 8912).pdf PDF document - 920.4 KB
  • Avis 8912 - NIPT

    French
    Mise en œuvre du screening génétique prénatal non invasif de la trisomie 21 (Syndrome de Down) dans la pratique des soins de santé en Belgique (mai 20.pdf PDF document - 1.06 MB

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