Publicaciones en colaboración con investigadores/as de Hospital Xeral Calde (2)

2010

  1. The genomics serving pediatrics in the investigation of the multifactorial disease

    Acta Pediatrica Espanola, Vol. 68, Núm. 2, pp. 55-60

2004

  1. A new rare mutation (691delCC/insAAA) in exon 17 of the PYGM gene causing McArdle disease

    Archives of Neurology, Vol. 61, Núm. 7, pp. 1108-1110