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Plos One|November 19, 2013
Prevalence of Lynch syndrome among patients with newly diagnosed endometrial cancersCecilia Egoavil, Cristina Alenda, Adela Castillejo, et al.
British Journal of Cancer|October 5, 2018
Primary constitutional MLH1 epimutations: a focal epigenetic eventEstela Dámaso, Adela Castillejo, María Del Mar Arias, et al.
Genetics in Medicine Open|June 15, 2026
RecQ DNA helicases germline variants in Lynch-like syndromeMar Giner-Calabuig, Seila De Leon, Gemma Vidal-Pedrola, et al.
Orphanet Journal of Rare Diseases|January 26, 2024
Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndromeAna Beatriz Sánchez-Heras, Estela Dámaso, Adela Castillejo, et al.
BMC Medical Genetics|January 21, 2011
Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndromeAdela Castillejo, Carla Guarinos, Ana Martinez-Canto, et al.
Human Molecular Genetics|February 7, 2014
New insights into POLE and POLD1 germline mutations in familial colorectal cancer and polyposisLaura Valle, Eva Hernández-Illán, Fernando Bellido, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 29, 2014
Prevalence and characteristics of MUTYH-associated polyposis in patients with multiple adenomatous and serrated polypsCarla Guarinos, Miriam Juárez, Cecilia Egoavil, et al.
Journal of Medical Genetics|April 25, 2015
Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancerAdela Castillejo, Eva Hernández-Illán, María Rodriguez-Soler, et al.
Cancers|November 10, 2020
Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic CharacterizationA Beatriz Sánchez-Heras, Adela Castillejo, Juan D García-Díaz, et al.
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