261 related articles for article (PubMed ID: 7795585)
1. Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444.
Caspari R; Olschwang S; Friedl W; Mandl M; Boisson C; Böker T; Augustin A; Kadmon M; Möslein G; Thomas G
Hum Mol Genet; 1995 Mar; 4(3):337-40. PubMed ID: 7795585
[TBL] [Abstract][Full Text] [Related]
2. Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis. Novel criteria of assessment and correlations with constitutional adenomatous polyposis coli gene mutations.
Valanzano R; Cama A; Volpe R; Curia MC; Mencucci R; Palmirotta R; Battista P; Ficari F; Mariani-Costantini R; Tonelli F
Cancer; 1996 Dec; 78(11):2400-10. PubMed ID: 8941012
[TBL] [Abstract][Full Text] [Related]
3. Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3' APC gene mutation.
Scott RJ; Froggatt NJ; Trembath RC; Evans DG; Hodgson SV; Maher ER
Hum Mol Genet; 1996 Dec; 5(12):1921-4. PubMed ID: 8968744
[TBL] [Abstract][Full Text] [Related]
4. Congenital hypertrophy of the retinal pigment epithelium and APC mutations in two Chinese families with familial adenomatous polyposis.
Pang CP; Keung JW; Tang NL; Fan DS; Lau JW; Lam DS
Eye (Lond); 2000 Feb; 14 ( Pt 1)():18-22. PubMed ID: 10755094
[TBL] [Abstract][Full Text] [Related]
5. A novel deletion at codon 441 of the APC gene associated with ophthalmic lesions (CHRPE) in a South African family.
Grobbelaar JJ; Ziskind A; de Jong G; Oosthuizen CJ; Kotze MJ
J Med Genet; 1996 May; 33(5):384-6. PubMed ID: 8733048
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. The relationship between congenital hypertrophy of the retinal pigment epithelium (CHRPE) and germline mutations in the adenomatous polyposis coli (APC) gene.
Ziskind A; Kitze MJ; Grobbelaar JJ
Ophthalmic Genet; 1999 Mar; 20(1):53-6. PubMed ID: 10454823
[No Abstract] [Full Text] [Related]
9. Congenital hypertrophy of the retinal pigment epithelium and APC mutations in Chinese with familial adenomatous polyposis.
Pang CP; Fan DS; Keung JW; Baum L; Tang NL; Lau JW; Lam DS
Ophthalmologica; 2001; 215(6):408-11. PubMed ID: 11741105
[TBL] [Abstract][Full Text] [Related]
10. Clinical findings in a family with familial adenomatous polyposis and a missense mutation of the adenomatous polyposis coli gene.
Marchese CA; Bertolino F; Ceccopieri B; Vanzetti M; Scaglione D; Locatelli L; Montera M; Romio L; Resta N; Stella A; Guanti G; Mareni C
Scand J Gastroenterol; 1996 Sep; 31(9):917-20. PubMed ID: 8888441
[TBL] [Abstract][Full Text] [Related]
11. Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis.
Bertario L; Russo A; Sala P; Eboli M; Giarola M; D'amico F; Gismondi V; Varesco L; Pierotti MA; Radice P;
Int J Cancer; 2001 Mar; 95(2):102-7. PubMed ID: 11241320
[TBL] [Abstract][Full Text] [Related]
12. The presence of congenital hypertrophy of the retinal pigment epithelium in a subgroup of patients with adenomatous polyposis coli mutations.
Reck AC; Bunyan D; Eccles D; Humphry R
Eye (Lond); 1997; 11 ( Pt 3)():298-300. PubMed ID: 9373466
[TBL] [Abstract][Full Text] [Related]
13. Congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial colorectal cancer.
Chen CS; Phillips KD; Grist S; Bennet G; Craig JE; Muecke JS; Suthers GK
Fam Cancer; 2006; 5(4):397-404. PubMed ID: 16944273
[TBL] [Abstract][Full Text] [Related]
14. Incidence and predictive value of congenital hypertrophy of retinal pigment epithelium in Chinese familial adenomatous polyposis patients.
Lam DS; Kwok SP; Kwok AK; Liew CT; Lau JW; Pang CC
Chin Med J (Engl); 1998 Mar; 111(3):278-81. PubMed ID: 10374435
[TBL] [Abstract][Full Text] [Related]
15. The most frequent APC mutations among Slovak familial adenomatous polyposis patients. Adenomatous polyposis coli.
Zajac V; Kovác M; Kirchhoff T; Stevurková V; Tomka M
Neoplasma; 2002; 49(6):356-61. PubMed ID: 12584582
[TBL] [Abstract][Full Text] [Related]
16. Ophthalmic and genetic screening in pedigrees with familial adenomatous polyposis.
Ruhswurm I; Zehetmayer M; Dejaco C; Wolf B; Karner-Hanusch J
Am J Ophthalmol; 1998 May; 125(5):680-6. PubMed ID: 9625552
[TBL] [Abstract][Full Text] [Related]
17. Mutations of adenomatous polyposis coli (APC) gene are uncommon in sporadic desmoid tumours.
Giarola M; Wells D; Mondini P; Pilotti S; Sala P; Azzarelli A; Bertario L; Pierotti MA; Delhanty JD; Radice P
Br J Cancer; 1998 Sep; 78(5):582-7. PubMed ID: 9744495
[TBL] [Abstract][Full Text] [Related]
18. Coexistence of somatic and germ-line mutations of APC gene in desmoid tumors from patients with familial adenomatous polyposis.
Miyaki M; Konishi M; Kikuchi-Yanoshita R; Enomoto M; Tanaka K; Takahashi H; Muraoka M; Mori T; Konishi F; Iwama T
Cancer Res; 1993 Nov; 53(21):5079-82. PubMed ID: 8221638
[TBL] [Abstract][Full Text] [Related]
19. Frequent mutations in the beta-catenin gene in desmoid tumors from patients without familial adenomatous polyposis.
Miyoshi Y; Iwao K; Nawa G; Yoshikawa H; Ochi T; Nakamura Y
Oncol Res; 1998; 10(11-12):591-4. PubMed ID: 10367940
[TBL] [Abstract][Full Text] [Related]
20. Desmoids and genotype in familial adenomatous polyposis.
Church J; Xhaja X; LaGuardia L; O'Malley M; Burke C; Kalady M
Dis Colon Rectum; 2015 Apr; 58(4):444-8. PubMed ID: 25751801
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
