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Annals of Oncology, ISSN 0923-7534, 10/2018, Volume 29, Issue suppl_7
Journal Article
Annals of Oncology, ISSN 0923-7534, 10/2017, Volume 28, Issue suppl_9
Journal Article
Gan to kagaku ryoho. Cancer & chemotherapy, ISSN 0385-0684, 07/2019, Volume 46, Issue 7, p. 1097
Lynch syndrome is one of the most common inherited predisposition syndromes which demonstrated autosomal dominant manner and is associated with increased risks... 
Genetic Predisposition to Disease | Exons | DNA Mismatch Repair | Humans | Female | Endometrial Neoplasms | Colorectal Neoplasms, Hereditary Nonpolyposis
Journal Article
Journal Article
by Thompson, Bryony A and Spurdle, Amanda B and Plazzer, John-Paul and Greenblatt, Marc S and Akagi, Kiwamu and Al-Mulla, Fahd and Bapat, Bharati and Bernstein, Inge and Capellá, Gabriel and den Dunnen, Johan T and du Sart, Desiree and Fabre, Aurelie and Farrell, Michael P and Farrington, Susan M and Frayling, Ian M and Frebourg, Thierry and Goldgar, David E and Heinen, Christopher D and Holinski-Feder, Elke and Kohonen-Corish, Maija and Robinson, Kristina Lagerstedt and Leung, Suet Yi and Martins, Alexana and Moller, Pal and Morak, Monika and Nystrom, Minna and Peltomaki, Paivi and Pineda, Marta and Qi, Ming and Ramesar, Rajkumar and Rasmussen, Lene Juel and Royer-Pokora, Brigitte and Scott, Rodney J and Sijmons, Rolf and Tavtigian, Sean V and Tops, Carli M and Weber, Thomas and Wijnen, Juul and Woods, Michael O and Macrae, Finlay and Genuardi, Maurizio and Castillejo, Adela and Sexton, Aienne and Chan, Anthony K. W and Viel, Alessana and Blanco, Amie and French, Amy and Laner, Aneas and Wagner, Anja and van den Ouweland, Ans and Mensenkamp, Arjen and Payá, Artemio and Betz, Beate and Redeker, Bert and Smith, Betsy and Espenschied, Carin and Cummings, Carole and Engel, Christoph and Fornes, Claudia and Valenzuela, Cristian and Alenda, Cristina and Buchanan, Daniel and Barana, Daniela and Konstantinova, Darina and Cairns, Dianne and Glaser, Elizabeth and Silva, Felipe and Lalloo, Fiona and Crucianelli, Francesca and Hogervorst, Frans and Casey, Graham and Tomlinson, Ian and Blanco, Ignacio and Villar, Isabel López and Garcia-Planells, Javier and Bigler, Jeanette and Shia, Jinru and Martinez-Lopez, Joaquin and Gille, Johan J. P and Hopper, John and Potter, John and Soto, José Luis and Kantelinen, Jukka and Ellis, Kate and Mann, Kirsty and Varesco, Liliana and Zhang, Liying and Le Marchand, Loic and Marafie, Makia J and Nordling, Margareta and Tibiletti, Maria Grazia and Kahan, Mariano Ariel and Ligtenberg, Marjolijn and Clendenning, Mark and Jenkins, Mark and Speevak, Marsha and Digweed, Martin and Kloor, Matthias and Hitchins, Megan and Myers, Megan and ... and InSiGHT and on behalf of InSiGHT and Sahlgrenska akademin and Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik and Göteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Medical and Clinical Genetics and Sahlgrenska Academy
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 2, pp. 107 - 115
Journal Article
世界胃肠病学杂志:英文版, ISSN 1007-9327, 2015, Volume 21, Issue 4, pp. 1275 - 1283
Journal Article
BRITISH JOURNAL OF CANCER, ISSN 0007-0920, 05/2019, Volume 120, Issue 10, pp. 982 - 986
BACKGROUND: OncoBEAM (TM) RAS CRC kit using BEAMing technology is a circulating tumour DNA (ctDNA) test for detecting plasma RAS mutational status in... 
ONCOLOGY | PLUS CETUXIMAB TREATMENT | MANAGEMENT | Plasma | Epidermal growth factor receptors | Colorectal carcinoma | Discordance | Colorectal cancer | Antibodies | Tissue analysis | Metastasis | Regression analysis | Tissues | Patients | Metastases | Lungs | Agreements | Mutation | Lesions | Deoxyribonucleic acid--DNA | Tumors | Cancer
Journal Article
Journal of Medical Case Reports, ISSN 1752-1947, 04/2019, Volume 13, Issue 1, pp. 117 - 6
DKC1 (dyskerin pseudouridine synthase 1) is a causative gene for X-linked dyskeratosis congenita. Approximately 8% of patients with dyskeratosis congenita have... 
X-linked recessive | Dyskeratosis congenita | Missense variant | Rectal cancer | DKC1 | RNA sequencing | Usage | Epithelial cells | Abnormalities | Colorectal cancer | Young men | Development and progression | Genetic aspects | Research | Health aspects | Immunoglobulins | Hematology | Anemia | Genes | Families & family life | Patients | Proteins | Hepatitis | Hemoglobin | Bone marrow | Blood pressure | Mutation | Endoscopy | Telomerase | Age | Cancer
Journal Article
British Journal of Cancer, ISSN 0007-0920, 11/2017, Volume 117, Issue 10, pp. 1450 - 1458
Journal Article
International Journal of Cancer, ISSN 0020-7136, 04/2016, Volume 138, Issue 7, pp. 1634 - 1644
Journal Article