[Prolonged neonatal hyperbilirubinemia associated with a UGT1A1 gene mutation].

Autor: de la Fuente Juárez A, Viñallonga Sardà X, Capdevila Cogul E, Porta Ribera R
Jazyk: Spanish; Castilian
Zdroj: Anales de pediatria (Barcelona, Spain : 2003) [An Pediatr (Barc)] 2010 Jun; Vol. 72 (6), pp. 449-50. Date of Electronic Publication: 2010 May 13.
DOI: 10.1016/j.anpedi.2010.03.002
Databáze: MEDLINE