229 related articles for article (PubMed ID: 19036155)
1. Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72.
Nilbert M; Kristoffersson U; Ericsson M; Johannsson O; Rambech E; Mangell P
BMC Med Genet; 2008 Nov; 9():101. PubMed ID: 19036155
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.
Stekrova J; Sulova M; Kebrdlova V; Zidkova K; Kotlas J; Ilencikova D; Vesela K; Kohoutova M
BMC Med Genet; 2007 Apr; 8():16. PubMed ID: 17411426
[TBL] [Abstract][Full Text] [Related]
4. Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families.
Friedl W; Caspari R; Sengteller M; Uhlhaas S; Lamberti C; Jungck M; Kadmon M; Wolf M; Fahnenstich J; Gebert J; Möslein G; Mangold E; Propping P
Gut; 2001 Apr; 48(4):515-21. PubMed ID: 11247896
[TBL] [Abstract][Full Text] [Related]
5. Phenotypic differences in familial adenomatous polyposis based on APC gene mutation status.
Heinimann K; Müllhaupt B; Weber W; Attenhofer M; Scott RJ; Fried M; Martinoli S; Müller H; Dobbie Z
Gut; 1998 Nov; 43(5):675-9. PubMed ID: 9824350
[TBL] [Abstract][Full Text] [Related]
6. The relationship between frequencies of extracolonic manifestations and the position of APC germline mutation in patients with familial adenomatous polyposis.
Enomoto M; Konishi M; Iwama T; Utsunomiya J; Sugihara KI; Miyaki M
Jpn J Clin Oncol; 2000 Feb; 30(2):82-8. PubMed ID: 10768871
[TBL] [Abstract][Full Text] [Related]
7. Variable phenotype of familial adenomatous polyposis in pedigrees with 3' mutation in the APC gene.
Brensinger JD; Laken SJ; Luce MC; Powell SM; Vance GH; Ahnen DJ; Petersen GM; Hamilton SR; Giardiello FM
Gut; 1998 Oct; 43(4):548-52. PubMed ID: 9824584
[TBL] [Abstract][Full Text] [Related]
8. APC germ-line mutations in southern Spanish patients with familial adenomatous polyposis: genotype-phenotype correlations and identification of eight novel mutations.
García-Lozano JR; Cordero C; Fernández-Suárez A; Encarnación M; Pizarro A; Núñez-Roldán A
Genet Test; 2005; 9(1):37-40. PubMed ID: 15857185
[TBL] [Abstract][Full Text] [Related]
9. Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): a review of the literature.
Nieuwenhuis MH; Vasen HF
Crit Rev Oncol Hematol; 2007 Feb; 61(2):153-61. PubMed ID: 17064931
[TBL] [Abstract][Full Text] [Related]
10. Mutation spectrum of the APC gene in 83 Korean FAP families.
Kim DW; Kim IJ; Kang HC; Park HW; Shin Y; Park JH; Jang SG; Yoo BC; Lee MR; Hong CW; Park KJ; Oh NG; Kim NK; Sung MK; Lee BW; Kim YJ; Lee H; Park JG
Hum Mutat; 2005 Sep; 26(3):281. PubMed ID: 16088911
[TBL] [Abstract][Full Text] [Related]
11. Variables affecting penetrance of gastric and duodenal phenotype in familial adenomatous polyposis patients.
Sample DC; Samadder NJ; Pappas LM; Boucher KM; Samowitz WS; Berry T; Westover M; Nathan D; Kanth P; Byrne KR; Burt RW; Neklason DW
BMC Gastroenterol; 2018 Jul; 18(1):115. PubMed ID: 30012100
[TBL] [Abstract][Full Text] [Related]
12. Genotype and phenotype of patients with both familial adenomatous polyposis and thyroid carcinoma.
Truta B; Allen BA; Conrad PG; Kim YS; Berk T; Gallinger S; Bapat B; Terdiman JP; Sleisenger MH
Fam Cancer; 2003; 2(2):95-9. PubMed ID: 14574158
[TBL] [Abstract][Full Text] [Related]
13. Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis.
Wallis YL; Macdonald F; Hultén M; Morton JE; McKeown CM; Neoptolemos JP; Keighley M; Morton DG
Hum Genet; 1994 Nov; 94(5):543-8. PubMed ID: 7959691
[TBL] [Abstract][Full Text] [Related]
14. Mutation cluster region, association between germline and somatic mutations and genotype-phenotype correlation in upper gastrointestinal familial adenomatous polyposis.
Groves C; Lamlum H; Crabtree M; Williamson J; Taylor C; Bass S; Cuthbert-Heavens D; Hodgson S; Phillips R; Tomlinson I
Am J Pathol; 2002 Jun; 160(6):2055-61. PubMed ID: 12057910
[TBL] [Abstract][Full Text] [Related]
15. Screening for mutations of the APC gene in 66 Italian familial adenomatous polyposis patients: evidence for phenotypic differences in cases with and without identified mutation.
Giarola M; Stagi L; Presciuttini S; Mondini P; Radice MT; Sala P; Pierotti MA; Bertario L; Radice P
Hum Mutat; 1999; 13(2):116-23. PubMed ID: 10094547
[TBL] [Abstract][Full Text] [Related]
16. A novel APC mutation identified in a large Chinese family with familial adenomatous polyposis and a brief literature review.
Pang M; Liu Y; Hou X; Yang J; He X; Hou N; Liu P; Liang L; Fu J; Wang K; Ye Z; Gong B
Mol Med Rep; 2018 Aug; 18(2):1423-1432. PubMed ID: 29901124
[TBL] [Abstract][Full Text] [Related]
17. APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis.
van der Luijt RB; Vasen HF; Tops CM; Breukel C; Fodde R; Meera Khan P
Hum Genet; 1995 Dec; 96(6):705-10. PubMed ID: 8522331
[TBL] [Abstract][Full Text] [Related]
18. The genetics of familial adenomatous polyposis (FAP) and MutYH-associated polyposis (MAP).
Claes K; Dahan K; Tejpar S; De Paepe A; Bonduelle M; Abramowicz M; Verellen C; Franchimont D; Van Cutsem E; Kartheuser A
Acta Gastroenterol Belg; 2011 Sep; 74(3):421-6. PubMed ID: 22103048
[TBL] [Abstract][Full Text] [Related]
19. Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis.
Bertario L; Russo A; Sala P; Varesco L; Giarola M; Mondini P; Pierotti M; Spinelli P; Radice P;
J Clin Oncol; 2003 May; 21(9):1698-707. PubMed ID: 12721244
[TBL] [Abstract][Full Text] [Related]
20. Familial adenomatous polyposis patients without an identified APC germline mutation have a severe phenotype.
Bisgaard ML; Ripa R; Knudsen AL; Bülow S
Gut; 2004 Feb; 53(2):266-70. PubMed ID: 14724162
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]