University of Erlangen-Nuremberg-ko ikertzaileekin lankidetzan egindako argitalpenak (2)

2015

  1. Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin–Siris and Nicolaides–Baraitser syndromes

    Human Genetics, Vol. 134, Núm. 6, pp. 553-568

2013

  1. A comprehensive molecular study on coffin-siris and nicolaides-baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling

    Human Molecular Genetics, Vol. 22, Núm. 25, pp. 5121-5135