Publicaciones en las que colabora con JOSE RAMON BILBAO CATALA (3)

2005

  1. A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain

    Pediatric Nephrology, Vol. 20, Núm. 7, pp. 891-896

2001

  1. Branchio-oto-renal syndrome: Identification of a novel mutation in the EYA1 gene

    Pediatric Nephrology, Vol. 16, Núm. 7, pp. 550-553

  2. Familial hypercalcemia and hypercalciuria: No mutations in the Ca2+-sensing receptor gene

    Pediatric Nephrology, Vol. 16, Núm. 9, pp. 748-751