المؤلفون: Iordache, Paul, Mates, Dana, Gunnarsson, Bjarni, Eggertsson, Hannes, sulem, patrick, Benonisdottir, Stefania, Csiki, Irma Eva, Rascu, Stefan, Radavoi, Daniel, Ursu, Radu, Staicu, Catalin, Calota, Violeta, Voinoiu, Angelica, Jinga, Mariana, Rosoga, Gabriel, Danau, Razvan, Sima, Sorin Cristian, Badescu, Daniel, Suciu, Nicoleta, Radoi, Viorica, Mates, Ioan Nicolae, Dobra, Mihai, Nicolae, Camelia, Kristjansdottir, Sigrun, Jónasson, Jón G., Manolescu, Andrei, Arnadottir, Gudny, Jensson, Brynjar Örn, Jonasdottir, Aslaug, Sigurdsson, Asgeir, le Roux, Louise, Johannsdottir, Hrefna, Rafnar, Thorunn, Halldórsson, Bjarni, Jinga, Viorel, Stefansson, Kari

المساهمون: Læknadeild (HÍ), Faculty of Medicine (UI), Tækni- og verkfræðideild (HR), School of Science and Engineering (RU), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Háskólinn í Reykjavík, Reykjavik University, Háskóli Íslands, University of Iceland

مصطلحات موضوعية: Colorectal cancer, Lynch syndrome, Romania, Endaþarmskrabbamein, Lynch heilkenni, Rúmenía

وصف الملف: 6068-6076

العلاقة: info:eu-repo/grantAgreement/EC/FP7/202059; Journal of Cellular and Molecular Medicine;22(12); Iordache, PD, Mates, D, Gunnarsson, B, et al. Identification of Lynch syndrome risk variants in the Romanian population. J Cell Mol Med. 2018; 22: 6068– 6076. https://doi.org/10.1111/jcmm.13881Test; 1582-4934 (eISSN); https://hdl.handle.net/20.500.11815/1301Test; Journal of Cellular and Molecular Medicine

الإتاحة: https://doi.org/20.500.11815/1301Test
https://doi.org/10.1111/jcmm.13881Test
https://hdl.handle.net/20.500.11815/1301Test

المؤلفون: Bjarni Gunnarsson, Viorel Jinga, Angelica Voinoiu, Hrefna Johannsdottir, Stefan Rascu, Stefania Benonisdottir, Violeta Calota, Sorin Cristian Sima, Jon G. Jonasson, Razvan Danau, Dana Mates, Viorica Radoi, Daniel Badescu, Radu Ursu, Camelia Nicolae, Gudny A. Arnadottir, Cătălin Alexandru Staicu, Bjarni V. Halldorsson, Thorunn Rafnar, Paul D. Iordache, Aslaug Jonasdottir, Asgeir Sigurdsson, Kari Stefansson, Mihai Dobra, Irma Eva Csiki, Hannes P. Eggertsson, Sigrun Kristjansdottir, Ioan Nicolae Mates, Mariana Jinga, Louise le Roux, Andrei Manolescu, Brynjar O. Jensson, Nicoleta Suciu, Daniel Radavoi, Gabriel Rosoga, Patrick Sulem

المساهمون: Læknadeild (HÍ), Faculty of Medicine (UI), Tækni- og verkfræðideild (HR), School of Science and Engineering (RU), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Háskólinn í Reykjavík, Reykjavik University, Háskóli Íslands, University of Iceland

المصدر: Journal of Cellular and Molecular Medicine

مصطلحات موضوعية: Male, 0301 basic medicine, Rúmenía, DNA Mismatch Repair, DNA Glycosylases, Risk Factors, PMS2, Mismatch Repair Endonuclease PMS2, Genetics, education.field_of_study, Middle Aged, Lynch syndrome, 3. Good health, DNA-Binding Proteins, MutS Homolog 2 Protein, Adenomatous Polyposis Coli, Molecular Medicine, Female, Original Article, MutL Protein Homolog 1, Adult, congenital, hereditary, and neonatal diseases and abnormalities, Lynch heilkenni, Population, Biology, MLH1, Familial adenomatous polyposis, 03 medical and health sciences, MUTYH, medicine, Humans, Genetic Predisposition to Disease, MLH1,MSH2,MSH6, MUTYH,PMS2, education, neoplasms, Aged, Endaþarmskrabbamein, Romania, nutritional and metabolic diseases, Original Articles, Cell Biology, DNA Methylation, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Colorectal cancer, digestive system diseases, MSH6, 030104 developmental biology, MSH2, Mutation

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beb71a9cd3010c7f038a6df677219bc6Test
https://doi.org/10.1111/jcmm.13881Test