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Alejandro Brea Fernández

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American Journal of Medical Genetics. Part A|December 21, 2018
Novel truncating variants expand the phenotypic spectrum of KAT6B-related disordersAlejandro Brea-Fernández, David Dacruz, Jesús Eirís, et al.
Revista De Enfermeria (Barcelona, Spain)|January 5, 2007
[Work responsibilities. Critical care unit]María Cristina Benítez Canosa, Alejandro Brea Fernández, Miguel Camino Castiñeiras, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|December 4, 2012
Vaginal tubulovillous adenoma: a clinicopathologic and molecular study with review of the literatureMaite Peña-Fernández, Ihab Abdulkader-Nallib, Alejandro Novo-Domínguez, et al.
Plos One|September 17, 2010
Single nucleotide polymorphisms in the Wnt and BMP pathways and colorectal cancer risk in a Spanish cohortCeres Fernández-Rozadilla, Luisa de Castro, Juan Clofent, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 10, 2010
Colorectal cancer susceptibility quantitative trait loci in mice as a novel approach to detect low-penetrance variants in humans: a two-stage case-control studyCeres Fernández-Rozadilla, Rosa Tarrío, Juan Clofent, et al.
Mutagenesis|February 2, 2012
Seeking genetic susceptibility variants for colorectal cancer: the EPICOLON consortium experienceSergi Castellví-Bel, Clara Ruiz-Ponte, Ceres Fernández-Rozadilla, et al.
European Journal of Human Genetics : EJHG|May 12, 2016
The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancerClara Esteban-Jurado, Sebastià Franch-Expósito, Jenifer Muñoz, et al.
BMC Genomics|January 29, 2013
A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12Ceres Fernandez-Rozadilla, Jean-Baptiste Cazier, Ian P Tomlinson, 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.
Gastroenterology|January 29, 2013
Risk of cancer in cases of suspected lynch syndrome without germline mutationMaría Rodríguez-Soler, Lucía Pérez-Carbonell, Carla Guarinos, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part A|December 21, 2018
Novel truncating variants expand the phenotypic spectrum of KAT6B-related disordersAlejandro Brea-Fernández, David Dacruz, Jesús Eirís, et al.
Revista De Enfermeria (Barcelona, Spain)|January 5, 2007
[Work responsibilities. Critical care unit]María Cristina Benítez Canosa, Alejandro Brea Fernández, Miguel Camino Castiñeiras, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|December 4, 2012
Vaginal tubulovillous adenoma: a clinicopathologic and molecular study with review of the literatureMaite Peña-Fernández, Ihab Abdulkader-Nallib, Alejandro Novo-Domínguez, et al.
Plos One|September 17, 2010
Single nucleotide polymorphisms in the Wnt and BMP pathways and colorectal cancer risk in a Spanish cohortCeres Fernández-Rozadilla, Luisa de Castro, Juan Clofent, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 10, 2010
Colorectal cancer susceptibility quantitative trait loci in mice as a novel approach to detect low-penetrance variants in humans: a two-stage case-control studyCeres Fernández-Rozadilla, Rosa Tarrío, Juan Clofent, et al.
Mutagenesis|February 2, 2012
Seeking genetic susceptibility variants for colorectal cancer: the EPICOLON consortium experienceSergi Castellví-Bel, Clara Ruiz-Ponte, Ceres Fernández-Rozadilla, et al.
European Journal of Human Genetics : EJHG|May 12, 2016
The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancerClara Esteban-Jurado, Sebastià Franch-Expósito, Jenifer Muñoz, et al.
BMC Genomics|January 29, 2013
A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12Ceres Fernandez-Rozadilla, Jean-Baptiste Cazier, Ian P Tomlinson, 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.
Gastroenterology|January 29, 2013
Risk of cancer in cases of suspected lynch syndrome without germline mutationMaría Rodríguez-Soler, Lucía Pérez-Carbonell, Carla Guarinos, et al.
Pageof 2