301 related articles for article (PubMed ID: 7959691)
1. 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]
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. 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]
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. Genotype-phenotype correlations of new causative APC gene mutations in patients with familial adenomatous polyposis.
Bunyan DJ; Shea-Simonds J; Reck AC; Finnis D; Eccles DM
J Med Genet; 1995 Sep; 32(9):728-31. PubMed ID: 8544194
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Fundus lesions of adenomatous polyposis.
Tiret A; Parc C
Curr Opin Ophthalmol; 1999 Jun; 10(3):168-72. PubMed ID: 10537774
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. Exceptions to the rule: individuals with FAP specific CHRPE and mutations in exon 6 of the APC gene.
Pack K; Smith-Ravin I; Phillips RK; Hodgson SV
Clin Genet; 1996 Aug; 50(2):110-1. PubMed ID: 8937774
[No Abstract] [Full Text] [Related]
13. Identification of APC exon 15 mutations in families suspected of familial adenomatous polyposis (FAP).
Kirchhoff T; Zajac V; Krizan P; Repiská V; Stevurková V; Friedl W
Folia Biol (Praha); 1997; 43(5):203-9. PubMed ID: 9595262
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Congenital hypertrophy of the retinal pigment epithelium serves as a clinical marker in a family with familial adenomatous polyposis.
Parisi ML
J Am Optom Assoc; 1995 Feb; 66(2):106-12. PubMed ID: 7714311
[TBL] [Abstract][Full Text] [Related]
17. Germline mutations of the APC gene in patients with familial adenomatous polyposis-associated thyroid carcinoma: results from a European cooperative study.
Cetta F; Montalto G; Gori M; Curia MC; Cama A; Olschwang S
J Clin Endocrinol Metab; 2000 Jan; 85(1):286-92. PubMed ID: 10634400
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Pigmented ocular fundus lesions and APC mutations in familial adenomatous polyposis.
Traboulsi EI; Apostolides J; Giardiello FM; Krush AJ; Booker SV; Hamilton SR; Hussels IE
Ophthalmic Genet; 1996 Dec; 17(4):167-74. PubMed ID: 9010867
[TBL] [Abstract][Full Text] [Related]
20. APC mutation and phenotypic spectrum of Singapore familial adenomatous polyposis patients.
Cao X; Eu KW; Seow-Choen F; Zao Y; Cheah PY
Eur J Hum Genet; 2000 Jan; 8(1):42-8. PubMed ID: 10713886
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
