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| Issue Date | Title | Author(s) |
|---|---|---|
| 12-Jan-2018 | A de novo FOXP1 truncating mutation in a patient originally diagnosed as C Syndrome | Urreizti, Roser; Damanti, Sarah; Esteve, Carla; Franco Valls, Héctor; Castilla Vallmanya, Laura; Tonda, Raul; Cormand Rifà, Bru; Vilageliu i Arqués, Lluïsa; Opitz, John M.; Neri, Giovanni; Grinberg Vaisman, Daniel Raúl; Balcells Comas, Susana |
| 10-Jul-2013 | Estratègies de diagnòstic genètic en fetus amb malformacions congènites. Correlació genotip-fenotip | Mademont Soler, Irene |
| 23-Sep-2010 | First trimester assessment of ductus venosus in screening for fetal chromosomal and cardiac defects | Maiz Elizaran, Nerea |
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