Jose-Ramírez, María; Pujol, Roser; Minguillon, Jordi; Bogliolo, Massimo; Persico, Ilaria; Cavero, Debora; de-la-Cal, Aurora; Rio, Paula; Navarro, Susana; Casado, José-Antonio; Bailador, Almudena; Sánchez-de-la-Fuente, Antonio; López-de-Heredia, Miguel; Almazan, Francisco; Antelo, María-Luisa; Argiles, Bienvenida; Badell, Isabel; Baragano, Marta; Belendez, Cristina; Bermudez-Cortés, Mar; Bernues, Marta; Isabel-Buedo, María; Carrasco, Estela; Catalá, Albert; Costa, Dolors; Cuesta, Isabel; Fernández-Delgado, Rafael; Fernández-Teijeir, Ana; Figuera, Ángela; García, Marta; Gondra, Ainhoa; González, Macarena; González-Muñiz, Soledad; Hernández-Rodríguez, Inés; Ibáñez, Fátima; John-Kelleher, Nicholas; Lendinez, Francisco; López, Mónica; López-Almaraz, Ricardo; Marchante, Inmaculada; Mendoza, Carmen; Nieto, José; Ojeda, Emilio; Payan-Pernia, Salvador; Peláez, Irene; Pérez-de-Soto, Inmaculada; Portugal, Raquel; Ramos-Arroyo, María-A; Regueiro, Alexandra; Rodríguez, Ana; Rosell, Jordi; Sáez, Raquel; Sánchez, José; Sánchez, Martha; Leónor-Senent, Ma; Tapia, María; Trujillo-Quintero, Juan-Pablo; Manuel-Vagace, José; Verdu-Amoros, Jaime; Verdugo, Victoria; Vidales, Isabel; Villarreal, Jasson; Díaz-de-Heredia, Cristina; Sevilla, Julián; Bueren, Juan-Antonio; Surralles, Jordi
(WILEY, 2025-02)
Fanconi anemia (FA) is a rare genetic disease characterized by high phenotypic and genotypic heterogeneity, and extreme chromosome fragility. To better understand the natural history of FA, identify genetic risk and ...