These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
221 related articles for article (PubMed ID: 34181357)
21. Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer. Carethers JM; Stoffel EM World J Gastroenterol; 2015 Aug; 21(31):9253-61. PubMed ID: 26309352 [TBL] [Abstract][Full Text] [Related]
22. Co-Occurrence of Germline Genomic Variants and Copy Number Variations in Hereditary Breast and Colorectal Cancer Patients. Côrtes L; Basso TR; Villacis RAR; Souza JDS; Jørgensen MMA; Achatz MI; Rogatto SR Genes (Basel); 2023 Aug; 14(8):. PubMed ID: 37628631 [TBL] [Abstract][Full Text] [Related]
23. Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing. Rohlin A; Rambech E; Kvist A; Törngren T; Eiengård F; Lundstam U; Zagoras T; Gebre-Medhin S; Borg Å; Björk J; Nilbert M; Nordling M Fam Cancer; 2017 Apr; 16(2):195-203. PubMed ID: 27696107 [TBL] [Abstract][Full Text] [Related]
24. Germline variants of uncertain significance, their frequency, and clinico-pathological features in a cohort of Sri Lankan patients with hereditary breast cancer. Gunawardena K; Sirisena ND; Anandagoda G; Neththikumara N; Dissanayake VHW BMC Res Notes; 2023 Jun; 16(1):95. PubMed ID: 37277882 [TBL] [Abstract][Full Text] [Related]
25. Copy number variants calling from WES data through eXome hidden Markov model (XHMM) identifies additional 2.5% pathogenic genomic imbalances smaller than 30 kb undetected by array-CGH. Tisserant E; Vitobello A; Callegarin D; Verdez S; Bruel AL; Aho Glele LS; Sorlin A; Viora-Dupont E; Konyukh M; Marle N; Nambot S; Moutton S; Racine C; Garde A; Delanne J; Tran-Mau-Them F; Philippe C; Kuentz P; Poulleau M; Payet M; Poe C; Thauvin-Robinet C; Faivre L; Mosca-Boidron AL; Thevenon J; Duffourd Y; Callier P Ann Hum Genet; 2022 Jul; 86(4):171-180. PubMed ID: 35141892 [TBL] [Abstract][Full Text] [Related]
26. Comprehensive molecular characterisation of hereditary non-polyposis colorectal tumours with mismatch repair proficiency. Bellido F; Pineda M; Sanz-Pamplona R; Navarro M; Nadal M; Lázaro C; Blanco I; Moreno V; Capellá G; Valle L Eur J Cancer; 2014 Jul; 50(11):1964-72. PubMed ID: 24841217 [TBL] [Abstract][Full Text] [Related]
27. Prevalence and characteristics of hereditary non-polyposis colorectal cancer (HNPCC) syndrome in immigrant Asian colorectal cancer patients. Lee J; Xiao YY; Sun YY; Balderacchi J; Clark B; Desani J; Kumar V; Saverimuthu A; Win KT; Huang Y; Xu Y BMC Cancer; 2017 Dec; 17(1):843. PubMed ID: 29237405 [TBL] [Abstract][Full Text] [Related]
28. Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis. de Leon MP; Pedroni M; Benatti P; Percesepe A; Di Gregorio C; Foroni M; Rossi G; Genuardi M; Neri G; Leonardi F; Viel A; Capozzi E; Boiocchi M; Roncucci L Gut; 1999 Jul; 45(1):32-8. PubMed ID: 10369701 [TBL] [Abstract][Full Text] [Related]
29. Detection of genetic alterations in gastric cancer patients from Saudi Arabia using comparative genomic hybridization (CGH). Bibi F; Ali I; Naseer MI; Ali Mohamoud HS; Yasir M; Alvi SA; Jiman-Fatani AA; Sawan A; Azhar EI PLoS One; 2018; 13(9):e0202576. PubMed ID: 30212456 [TBL] [Abstract][Full Text] [Related]
30. Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGH. Hackmann K; Kuhlee F; Betcheva-Krajcir E; Kahlert AK; Mackenroth L; Klink B; Di Donato N; Tzschach A; Kast K; Wimberger P; Schrock E; Rump A Breast Cancer Res Treat; 2016 Oct; 159(3):585-90. PubMed ID: 27581129 [TBL] [Abstract][Full Text] [Related]
31. Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencing. Mancini-DiNardo D; Judkins T; Kidd J; Bernhisel R; Daniels C; Brown K; Meek K; Craft J; Holladay J; Morris B; Roa BB BMC Med Genomics; 2019 Oct; 12(1):138. PubMed ID: 31623605 [TBL] [Abstract][Full Text] [Related]
32. Suspected hereditary nonpolyposis colorectal cancer: International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) criteria and results of genetic diagnosis. Park JG; Vasen HF; Park KJ; Peltomaki P; Ponz de Leon M; Rodriguez-Bigas MA; Lubinski J; Beck NE; Bisgaard ML; Miyaki M; Wijnen JT; Baba S; Lynch HT Dis Colon Rectum; 1999 Jun; 42(6):710-5; discussion 715-6. PubMed ID: 10378593 [TBL] [Abstract][Full Text] [Related]
33. Copy number variation in Fayoumi and Leghorn chickens analyzed using array comparative genomic hybridization. Abernathy J; Li X; Jia X; Chou W; Lamont SJ; Crooijmans R; Zhou H Anim Genet; 2014 Jun; 45(3):400-11. PubMed ID: 24628374 [TBL] [Abstract][Full Text] [Related]
35. Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts. Devlin LA; Graham CA; Price JH; Morrison PJ Ulster Med J; 2008 Jan; 77(1):25-30. PubMed ID: 18269114 [TBL] [Abstract][Full Text] [Related]
37. Copy Number Variants Are Enriched in Individuals With Early-Onset Obesity and Highlight Novel Pathogenic Pathways. Pettersson M; Viljakainen H; Loid P; Mustila T; Pekkinen M; Armenio M; Andersson-Assarsson JC; Mäkitie O; Lindstrand A J Clin Endocrinol Metab; 2017 Aug; 102(8):3029-3039. PubMed ID: 28605459 [TBL] [Abstract][Full Text] [Related]
38. Characterization of germline copy number variation in high-risk African American families with prostate cancer. Ledet EM; Hu X; Sartor O; Rayford W; Li M; Mandal D Prostate; 2013 May; 73(6):614-23. PubMed ID: 23060098 [TBL] [Abstract][Full Text] [Related]
40. The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer. Malander S; Rambech E; Kristoffersson U; Halvarsson B; Ridderheim M; Borg A; Nilbert M Gynecol Oncol; 2006 May; 101(2):238-43. PubMed ID: 16360201 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]