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2. Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases. Spier I; Drichel D; Kerick M; Kirfel J; Horpaopan S; Laner A; Holzapfel S; Peters S; Adam R; Zhao B; Becker T; Lifton RP; Perner S; Hoffmann P; Kristiansen G; Timmermann B; Nöthen MM; Holinski-Feder E; Schweiger MR; Aretz S J Med Genet; 2016 Mar; 53(3):172-9. PubMed ID: 26613750 [TBL] [Abstract][Full Text] [Related]
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4. Unexplained polyposis: a challenge for geneticists, pathologists and gastroenterologists. Mongin C; Coulet F; Lefevre JH; Colas C; Svrcek M; Eyries M; Lahely Y; Fléjou JF; Soubrier F; Parc Y Clin Genet; 2012 Jan; 81(1):38-46. PubMed ID: 21476993 [TBL] [Abstract][Full Text] [Related]
6. Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients. Elsayed FA; Tops CMJ; Nielsen M; Morreau H; Hes FJ; van Wezel T Fam Cancer; 2022 Jan; 21(1):79-83. PubMed ID: 33683519 [TBL] [Abstract][Full Text] [Related]
7. Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary. Papp J; Kovacs ME; Matrai Z; Orosz E; Kásler M; Børresen-Dale AL; Olah E Fam Cancer; 2016 Jan; 15(1):85-97. PubMed ID: 26446593 [TBL] [Abstract][Full Text] [Related]
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10. Mutation Spectrum of Familial Adenomatous Polyposis Patients in Turkish Population: Identification of 3 Novel APC Mutations. Arslan Ateş E; Alavanda C; Demir Ş; Keklikkıran Ç; Attaallah W; Özdoğan OC; Güney Aİ Turk J Gastroenterol; 2022 Feb; 33(2):81-87. PubMed ID: 35238777 [TBL] [Abstract][Full Text] [Related]
11. Detection of APC mosaicism by next-generation sequencing in an FAP patient. Yamaguchi K; Komura M; Yamaguchi R; Imoto S; Shimizu E; Kasuya S; Shibuya T; Hatakeyama S; Takahashi N; Ikenoue T; Hata K; Tsurita G; Shinozaki M; Suzuki Y; Sugano S; Miyano S; Furukawa Y J Hum Genet; 2015 May; 60(5):227-31. PubMed ID: 25716913 [TBL] [Abstract][Full Text] [Related]
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13. Somatic APC mosaicism: an underestimated cause of polyposis coli. Hes FJ; Nielsen M; Bik EC; Konvalinka D; Wijnen JT; Bakker E; Vasen HF; Breuning MH; Tops CM Gut; 2008 Jan; 57(1):71-6. PubMed ID: 17604324 [TBL] [Abstract][Full Text] [Related]
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16. Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis. Nielsen M; Hes FJ; Nagengast FM; Weiss MM; Mathus-Vliegen EM; Morreau H; Breuning MH; Wijnen JT; Tops CM; Vasen HF Clin Genet; 2007 May; 71(5):427-33. PubMed ID: 17489848 [TBL] [Abstract][Full Text] [Related]
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19. Colorectal Adenomatous Polyposis: Heterogeneity of Susceptibility Gene Mutations and Phenotypes in a Cohort of Italian Patients. Marabelli M; Molinaro V; Abou Khouzam R; Berrino E; Panero M; Balsamo A; Venesio T; Ranzani GN Genet Test Mol Biomarkers; 2016 Dec; 20(12):777-785. PubMed ID: 27705013 [TBL] [Abstract][Full Text] [Related]
20. Colorectal adenomatous polyposis syndromes: Genetic determinism, clinical presentation and recommendations for care. Buecher B Bull Cancer; 2016 Feb; 103(2):199-209. PubMed ID: 26805944 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]