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
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

Advise 8912 - NIPT