XV-2c and KM: 19 haplotype analysis in Chilean patients with cystic fibrosis and unknown CFTR gene mutations

por REPETTO,GABRIELA M, PUGA,ALONSO R, DELGADO,IRIS
Publicado 2007

VEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based study

por CALDERÓN,JUAN FRANCISCO, PUGA,ALONSO R, GUZMÁN,M. LUISA, ASTETE,CARMEN PAZ, ARRIAZA,MARTA, ARACENA,MARIANA, ARAVENA,TERESA, SANZ,PATRICIA, REPETTO,GABRIELA M
Publicado 2009