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| Issue Date | Title | Author(s) |
|---|---|---|
| 25-Sep-2023 | Chromosomal instability-induced cell invasion through caspase-driven DNA damage | Barrio, Lara; Gaspar, Ana Elena; Muzzopappa, Mariana; Ghosh, Kaustuv; Romão, Daniela; Clemente Ruiz, Marta; Milán, Marco |
| 30-Jul-2021 | Lung Transplant Improves Survival and Quality of Life Regardless of Telomere Dysfunction | Planas Cerezales, Lurdes; Arias Salgado, Elena G.; Berastegui, Cristina; Montes Worboys, Ana; González Montelongo, Rafaela; Lorenzo Salazar, José. M.; Vicens Zygmunt, Vanesa; García Moyano, Marta; Dorca i Sargatal, Jordi; Flores, Carlos; Perona, Rosario; Román, Antonio; Molina Molina, María |
| 3-Jul-2022 | Very long time persistent hyperCKemia as the first manifestation of McLeod syndrome: a case report. | Torres, Viviana; Painous Martí, Cèlia; Santacruz, Pilar; Sánchez, Aurora; Sanz, Cristina; Grau Junyent, Josep M. (Josep Maria); Muñoz, Esteban |
| 17-Sep-2021 | Pleiotropic effects of candidate genes on autism spectrum disorder and comorbidities: genetics, funcional studies and animal models | Antón Galindo, Ester |
| 27-Jul-2023 | Mutational Profile Enables the Identification of a High-Risk Subgroup in Myelodysplastic Syndromes with Isolated Trisomy 8 | Toribio Castelló, Sofía; Castaño, Sandra; Villaverde Ramiro, Ángela; Such, Esperanza; Arnán, Montserrat; Solé, Francesc; Díaz Beyà, Marina; Díez Campelo, María; Rey, Mónica del; González, Teresa; Hernández Rivas, Jesús María |
| Apr-1998 | Factores nocivos para el desarrollo de la gestación | Francés Ribera, Lidia |
| 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 |
| Aug-2001 | Características y tratamiento estomatológico en la trisomía parcial del cromosoma nº 9. | López Jiménez, Julián; Romero Domínguez, Andrés; Giménez Prats, Mª José; Chimenos Küstner, Eduardo |
| 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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