Publications by the researcher in collaboration with Encarnacion Guillen Navarro (3)

2008

  1. Review of 22 patients with 22q11.2 deletion syndrome: Phenotype spectrum

    Anales de Pediatria, Vol. 69, Núm. 4, pp. 304-310

2004

  1. Novel HMBS founder mutation and significant intronic polymorphism in Spanish patients with acute intermittent porphyria

    Annals of Human Genetics, Vol. 68, Núm. 5, pp. 509-514

1995

  1. SINDROME DE SHOCK TOXICO. PRESENTACION DE DOS CASOS EN LACTANTES

    Anales Espanoles de Pediatria, Vol. 42, Núm. 5, pp. 361-364