Publikationen in Zusammenarbeit mit Forschern von Vall d'Hebron Institut de Recerca (1)

2013

  1. Trisomy 18p caused by a supernumerary marker with a chromosome 13/21 centromere: A possible recurrent chromosome aberration

    American Journal of Medical Genetics, Part A, Vol. 161, Núm. 9, pp. 2363-2368