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G Llort

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

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Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 9, 2015
Automatic registration of pre- and intraoperative data for long bones in minimally invasive surgeryH E Fakhfakh, G Llort-Pujol, C Hamitouche, et al.
Genes, Chromosomes & Cancer|January 9, 2008
Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in the MSH2 geneM Pineda, E Castellsagué, E Musulén, et al.
Breast Cancer Research and Treatment|April 7, 2010
Copy number variations are not modifiers of phenotypic expression in a pair of identical twins carrying a BRCA1 mutationA Lasa, T Ramón y Cajal, G Llort, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|December 17, 2015
SEOM clinical guidelines in Hereditary Breast and ovarian cancerG Llort, I Chirivella, R Morales, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|January 15, 2015
Two novel frameshift mutations in BRCA2 gene detected by next generation sequencing in a survey of Spanish patients of breast cancerI Hernan, B Mañé, E Borràs, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|January 1, 2020
SEOM clinical guidelines in hereditary breast and ovarian cancer (2019)S González-Santiago, T Ramón Y Cajal, E Aguirre, et al.
Gastroenterologia Y Hepatologia|January 6, 2006
[Current status of follow-up of the upper digestive tract in familial adenomatous polyposis]D Parés, A García-Ruiz, S Biondo, et al.
British Journal of Cancer|October 15, 2009
Gene expression profiling integrated into network modelling reveals heterogeneity in the mechanisms of BRCA1 tumorigenesisR Fernández-Ramires, X Solé, L De Cecco, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|August 29, 2013
Association of BRCA1 germline mutations in young onset triple-negative breast cancer (TNBC)R Andrés, I Pajares, J Balmaña, et al.
British Journal of Cancer|September 11, 2008
An evaluation of the polymorphisms Ins16bp and Arg72Pro in p53 as breast cancer risk modifiers in BRCA1 and BRCA2 mutation carriersA Osorio, M Pollán, G Pita, et al.
Pageof 2

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

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Pageof 2
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 9, 2015
Automatic registration of pre- and intraoperative data for long bones in minimally invasive surgeryH E Fakhfakh, G Llort-Pujol, C Hamitouche, et al.
Genes, Chromosomes & Cancer|January 9, 2008
Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in the MSH2 geneM Pineda, E Castellsagué, E Musulén, et al.
Breast Cancer Research and Treatment|April 7, 2010
Copy number variations are not modifiers of phenotypic expression in a pair of identical twins carrying a BRCA1 mutationA Lasa, T Ramón y Cajal, G Llort, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|December 17, 2015
SEOM clinical guidelines in Hereditary Breast and ovarian cancerG Llort, I Chirivella, R Morales, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|January 15, 2015
Two novel frameshift mutations in BRCA2 gene detected by next generation sequencing in a survey of Spanish patients of breast cancerI Hernan, B Mañé, E Borràs, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|January 1, 2020
SEOM clinical guidelines in hereditary breast and ovarian cancer (2019)S González-Santiago, T Ramón Y Cajal, E Aguirre, et al.
Gastroenterologia Y Hepatologia|January 6, 2006
[Current status of follow-up of the upper digestive tract in familial adenomatous polyposis]D Parés, A García-Ruiz, S Biondo, et al.
British Journal of Cancer|October 15, 2009
Gene expression profiling integrated into network modelling reveals heterogeneity in the mechanisms of BRCA1 tumorigenesisR Fernández-Ramires, X Solé, L De Cecco, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|August 29, 2013
Association of BRCA1 germline mutations in young onset triple-negative breast cancer (TNBC)R Andrés, I Pajares, J Balmaña, et al.
British Journal of Cancer|September 11, 2008
An evaluation of the polymorphisms Ins16bp and Arg72Pro in p53 as breast cancer risk modifiers in BRCA1 and BRCA2 mutation carriersA Osorio, M Pollán, G Pita, et al.
Pageof 2