Publikationen in Zusammenarbeit mit Forschern von Dalhousie University (2)

2020

  1. Systematic review and network meta-analysis with individual participant data on cord management at preterm birth (iCOMP): Study protocol

    BMJ Open, Vol. 10, Núm. 3

2014

  1. Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

    Human Molecular Genetics, Vol. 23, Núm. 11, pp. 2888-2900