Cornelia de Lange Syndrome: Antenatal diagnosis in two consecutive pregnancies due to rare gonadal mosaicism of NIPBL gene mutation

Jan Weichert*, Andreas Schröer, Daniel Alexander Beyer, Gabriele Gillessen-Kaesbach, Irina Stefanova

*Corresponding author for this work
    4 Citations (Scopus)

    Fingerprint

    Dive into the research topics of 'Cornelia de Lange Syndrome: Antenatal diagnosis in two consecutive pregnancies due to rare gonadal mosaicism of NIPBL gene mutation'. Together they form a unique fingerprint.

    Medicine & Life Sciences