Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Colorectal Neoplasms and BLM[original query] |
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Heterozygosity for the BLM(Ash) mutation and cancer risk. Cancer research 2003 Apr 63 (8): 1769-71. Cleary Sean P, Zhang William, Di Nicola Nando, Aronson Melyssa, Aube Jennifer, Steinman Amanda, Haddad Riad, Redston Mark, Gallinger Steven, Narod Steven A, Gryfe Robe |
Coinheritance of BRCA1 and BRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: possible role in risk modification for cancer development. American journal of hematology 2005 Mar 78 (3): 203-6. Koren-Michowitz M, Friedman E, Gershoni-Baruch R, Brok-Simoni F, Patael Y, Rechavi G, Amariglio |
Colorectal cancer and polymorphisms in DNA repair genes WRN, RMI1 and BLM. Carcinogenesis 2010 Mar 31 (3): 442-5. Frank Bernd, Hoffmeister Michael, Klopp Norman, Illig Thomas, Chang-Claude Jenny, Brenner Herma |
Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer. Scientific reports 2015 5 14060. de Voer Richarda M, Hahn Marc-Manuel, Mensenkamp Arjen R, Hoischen Alexander, Gilissen Christian, Henkes Arjen, Spruijt Liesbeth, van Zelst-Stams Wendy A, Marleen Kets C, Verwiel Eugene T, Nagtegaal Iris D, Schackert Hans K, van Kessel Ad Geurts, Hoogerbrugge Nicoline, Ligtenberg Marjolijn J L, Kuiper Roland |
The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers. Cancer genetics 2015 Dec . Laitman Yael, Boker-Keinan Lital, Berkenstadt Michal, Liphsitz Irena, Weissglas-Volkov Daphna, Ries-Levavi Liat, Sarouk Ifat, Pras Elon, Friedman Eit |
Colorectal and Endometrial Cancer Risk and Age at Diagnosis in BLMAsh Mutation Carriers. The Israel Medical Association journal : IMAJ 2017 Jun 19 (6): 365-367. Schayek Hagit, Laitman Yael, Katz Lior H, Pras Elon, Ries-Levavi Liat, Barak Frida, Friedman Eit |
Integrated Analysis of Germline and Tumor DNA Identifies New Candidate Genes Involved in Familial Colorectal Cancer. Cancers 2019 Mar 11 (3): . Díaz-Gay Marcos, Franch-Expósito Sebastià, Arnau-Collell Coral, Park Solip, Supek Fran, Muñoz Jenifer, Bonjoch Laia, Gratacós-Mulleras Anna, Sánchez-Rojas Paula A, Esteban-Jurado Clara, Ocaña Teresa, Cuatrecasas Miriam, Vila-Casadesús Maria, Lozano Juan José, Parra Genis, Laurie Steve, Beltran Sergi, , Castells Antoni, Bujanda Luis, Cubiella Joaquín, Balaguer Francesc, Castellví-Bel Ser |
A comprehensive custom panel evaluation for routine hereditary cancer testing: improving the yield of germline mutation detection. Journal of translational medicine 2020 Jun 18 (1): 232. Velázquez Carolina, Lastra Enrique, Avila Cobos Francisco, Abella Luis, de la Cruz Virginia, Hernando Blanca Ascensión, Hernández Lara, Martínez Noemí, Infante Mar, Durán Merced |
Candidate genes for hereditary colorectal cancer: Mutational screening and systematic review. Human mutation 2020 May . Belhadj Sami, Terradas Mariona, Munoz-Torres Pau M, Aiza Gemma, Navarro Matilde, Capellá Gabriel, Valle Lau |
[Difference analysis of somatic mutations between deficient mismatch repair and proficient mismatch repair gene related with colorectal cancer]. Zhonghua zhong liu za zhi [Chinese journal of oncology] 2021 10 43 (10): 1088-1093. Tang X J, Yang M Y, Zhu L Z, Xu D, Yuan |
The prevalence of germline pathogenic variants in Estonian colorectal cancer patients: results from routine clinical setting 2016-2021. Frontiers in genetics 2022 11 13 1020543. Roht Laura, Tooming Mikk, Rekker Kadri, Roomere Hanno, Toome Kadri, Murumets Ülle, Šamarina Ustina, Õunap Katrin, Kahre Tii |
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