Publicaciones en colaboración con investigadores/as de University of Freiburg (1)

2012

  1. Miller (genéeacute;wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH

    Human Molecular Genetics, Vol. 21, Núm. 18, pp. 3969-3983