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Acceso abierto2017_Ferrer-Avargues_etal_JGeneMed_final.pdf.jpgd’abril-2017Characterization of a novel POLD1 missense founder mutation in a Spanish populationFerrer‐Avargues, Rosario; Díez‐Obrero, Virginia; Martín‐Tomás, Ester, et al
Acceso restringidoEpcam.pdf.jpg6-de novembre-2010EPCAM germ line deletions as causes of Lynch Syndrome in Spanish patientsGuarinos, Carla; Castillejo, Adela; Barberá, Víctor Manuel, et al
Acceso abiertoBMC Medical Genetics.pdf.jpg19-de gener-2011Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndromeCastillejo, Adela; Guarinos, Carla; Martínez-Cantó, Ana, et al
Acceso abiertoSanchez-Heras_etal_2020_Cancers.pdf.jpg5-de novembre-2020Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic CharacterizationSánchez-Heras, Ana Beatriz; Castillejo, Adela; García-Díaz, Juan D., et al
Acceso abierto2013_Egoavil_etal_PLoS_ONE.pdf.jpg7-de novembre-2013Prevalence of Lynch Syndrome among Patients with Newly Diagnosed Endometrial CancersEgoavil, Cecilia; Alenda, Cristina; Castillejo, Adela, et al
Acceso restringido2015_Castillejo_etal_JMedGenet_final.pdf.jpg23-d’abril-2015Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancerCastillejo, Adela; Hernández Illán, Eva; Rodríguez-Soler, María, et al
Acceso restringido2012_Castillejo_etal_JCO.pdf.jpgd’agost-2012Recurrent Testicular Germ Cell Tumors in a Family With MYH-Associated PolyposisCastillejo, Adela; Sánchez-Heras, Ana Beatriz; Jover, Rodrigo, et al
Acceso abiertoPico_etal_2020_Cancers.pdf.jpg9-d’agost-2020Risk of Cancer in Family Members of Patients with Lynch-Like SyndromePicó, María Dolores; Sánchez-Heras, Ana Beatriz; Castillejo, Adela, et al
Acceso abiertoGuillen-Ponce_etal_2020_ClinTranslOncol.pdf.jpgde febrer-2020SEOM clinical guideline on hereditary colorectal cancer (2019)Guillén-Ponce, Carmen; Lastra, Enrique; Lorenzo-Lorenzo, Isabel, et al