Prenatally detected copy number variants in a national cohort: A postnatal follow-up study.
Joke MuysYves JacquemynBettina BlaumeiserLaura BourlardNathalie BrisonSaskia BulkPatrizia ChiarappaAnne De LeenerMarjan De RademaekerJulie DésirAnne DestréeKoenraad DevriendtAnnelies DheedeneArmelle DuquenneAnnelies FieuwErik FransenJean-Stéphane GatotMauricette JamarSandra JanssensJorien KerstjensKathelijn KeymolenDamien LedererBjörn MentenBruno PichonSonia RomboutYves SznajerAnn Van Den BogaertKris Van Den BogaertJoris VermeeschKatrien JanssensPublished in: Prenatal diagnosis (2020)
Our postnatal follow-up project of children with a prenatally detected non-benign CNV is the first nationwide project of its kind. A higher number of cases for each CNV category is however needed to confirm our findings.