Advise 8912 - NIPT | FÖD Volksgesundheit

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)

Advies 8912 - NIPT
Niederländisch
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
Französisch
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
Englisch
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

Avis 8912 - NIPT

Advise 8912 - NIPT