Advise 8912 - NIPT | FPS Public Health

18/03/2015

Implementation of non-invasive prenatal genetic screening for trisomy 21 (Down Syndrome) in the practice of health care in Belgium (May 2014) (SHC 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

Advise 8912 - NIPT

Advies 8912 - NIPT

Avis 8912 - NIPT