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.
175 related articles for article (PubMed ID: 21901790)
1. Novel LOVD databases for hereditary breast cancer and colorectal cancer genes in the Chinese population. Pan M; Cong P; Wang Y; Lin C; Yuan Y; Dong J; Banerjee S; Zhang T; Chen Y; Zhang T; Chen M; Hu P; Zheng S; Zhang J; Qi M Hum Mutat; 2011 Dec; 32(12):1335-40. PubMed ID: 21901790 [TBL] [Abstract][Full Text] [Related]
2. Pancreatic Cancer with Mutation in BRCA1/2, MLH1, and APC Genes: Phenotype Correlation and Detection of a Novel Germline BRCA2 Mutation. Vietri MT; D'Elia G; Caliendo G; Albanese L; Signoriello G; Napoli C; Molinari AM Genes (Basel); 2022 Feb; 13(2):. PubMed ID: 35205366 [TBL] [Abstract][Full Text] [Related]
4. A novel pathogenic splice acceptor site germline mutation in intron 14 of the APC gene in a Chinese family with familial adenomatous polyposis. Wang D; Liang S; Zhang Z; Zhao G; Hu Y; Liang S; Zhang X; Banerjee S Oncotarget; 2017 Mar; 8(13):21327-21335. PubMed ID: 28423518 [TBL] [Abstract][Full Text] [Related]
6. Genotype to phenotype: analyzing the effects of inherited mutations in colorectal cancer families. Heinen CD Mutat Res; 2010 Nov; 693(1-2):32-45. PubMed ID: 19766128 [TBL] [Abstract][Full Text] [Related]
7. [Gene mutations in and physiopathology of familial adenomatous polyposis and hereditary non-polyposis colorectal cancer]. Iwama T Nihon Naika Gakkai Zasshi; 2007 Feb; 96(2):207-12. PubMed ID: 17370583 [No Abstract] [Full Text] [Related]
9. Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests. Pujol P; Lyonnet DS; Frebourg T; Blin J; Picot MC; Lasset C; Dugast C; Berthet P; de Paillerets BB; Sobol H; Grandjouan S; Soubrier F; Buecher B; Guimbaud R; Lidereau R; Jonveaux P; Houdayer C; Giraud S; Olschwang S; Nogue E; Galibert V; Bara C; Nowak F; Khayat D; Nogues C Breast Cancer Res Treat; 2013 Aug; 141(1):135-44. PubMed ID: 23974829 [TBL] [Abstract][Full Text] [Related]
10. Next Generation Sequencing Reveals Novel Mutations in Mismatch Repair Genes and Other Cancer Predisposition Genes in Asian Patients with Suspected Lynch Syndrome. Ow SGW; Tan KT; Yang H; Yap HL; Sapari NSB; Ong PY; Soong R; Lee SC Clin Colorectal Cancer; 2019 Dec; 18(4):e324-e334. PubMed ID: 31350202 [TBL] [Abstract][Full Text] [Related]
11. Familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC): a review of clinical, genetic and therapeutic aspects. Soravia C; Bapat B; Cohen Z Schweiz Med Wochenschr; 1997 Apr; 127(16):682-90. PubMed ID: 9140167 [TBL] [Abstract][Full Text] [Related]
12. Mismatch repair gene mutation analysis and colonoscopy surveillance in Chinese Lynch syndrome families. Fu L; Sheng JQ; Li XO; Jin P; Mu H; Han M; Huang JS; Sun ZQ; Li AQ; Wu ZT; Li SR Cell Oncol (Dordr); 2013 Jun; 36(3):225-31. PubMed ID: 23640085 [TBL] [Abstract][Full Text] [Related]
14. Identification of a comprehensive spectrum of genetic factors for hereditary breast cancer in a Chinese population by next-generation sequencing. Yang X; Wu J; Lu J; Liu G; Di G; Chen C; Hou Y; Sun M; Yang W; Xu X; Zhao Y; Hu X; Li D; Cao Z; Zhou X; Huang X; Liu Z; Chen H; Gu Y; Chi Y; Yan X; Han Q; Shen Z; Shao Z; Hu Z PLoS One; 2015; 10(4):e0125571. PubMed ID: 25927356 [TBL] [Abstract][Full Text] [Related]
15. Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry. Casey MJ; Bewtra C; Lynch HT; Snyder C; Stacy M; Watson P Fam Cancer; 2013 Dec; 12(4):719-40. PubMed ID: 23666231 [TBL] [Abstract][Full Text] [Related]
16. Adenomatous Polyposis Coli Gene Mutations in 22 Chinese Pedigrees with Familial Adenomatous Polyposis. Wang D; Zhang Z; Li Y; Xu C; Yu Y; Li M; Chen C; Zhang X Med Sci Monit; 2019 May; 25():3796-3803. PubMed ID: 31113927 [TBL] [Abstract][Full Text] [Related]
17. Hereditary colorectal cancer syndromes: familial adenomatous polyposis and lynch syndrome. Al-Sukhni W; Aronson M; Gallinger S Surg Clin North Am; 2008 Aug; 88(4):819-44, vii. PubMed ID: 18672142 [TBL] [Abstract][Full Text] [Related]
18. A novel pathogenic germline mutation in the adenomatous polyposis coli gene in a Chinese family with familial adenomatous coli. Jiang SS; Li JJ; Li Y; He LJ; Wang QJ; Weng DS; Pan K; Liu Q; Zhao JJ; Pan QZ; Zhang XF; Tang Y; Chen CL; Zhang HX; Xu GL; Zeng YX; Xia JC Oncotarget; 2015 Sep; 6(29):27267-74. PubMed ID: 26311738 [TBL] [Abstract][Full Text] [Related]
19. Pathology of the hereditary colorectal carcinoma. Gatalica Z; Torlakovic E Fam Cancer; 2008; 7(1):15-26. PubMed ID: 17564815 [TBL] [Abstract][Full Text] [Related]
20. Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC. Laken SJ; Petersen GM; Gruber SB; Oddoux C; Ostrer H; Giardiello FM; Hamilton SR; Hampel H; Markowitz A; Klimstra D; Jhanwar S; Winawer S; Offit K; Luce MC; Kinzler KW; Vogelstein B Nat Genet; 1997 Sep; 17(1):79-83. PubMed ID: 9288102 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]