147 related articles for article (PubMed ID: 8937774)
1. 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]
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 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]
4. 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]
5. 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]
6. Rapid RT-PCR-based protein truncation test in the screening for 5' located mutations of the APC gene.
Kraus C; Günther K; Vogler A; Hohenberger W; Pfeiffer RA; Ballhausen WG
Mol Cell Probes; 1998 Jun; 12(3):143-7. PubMed ID: 9664575
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. [Congenital hypertrophy of retinal pigment epithelium: a marker in familial adenomatous polyposis].
Szwarcberg J; Limacher JM; Fricker JP; Flament J
J Fr Ophtalmol; 1999 Apr; 22(3):364-70. PubMed ID: 10337595
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Different familial adenomatous polyposis phenotypes resulting from deletions of the entire APC exon 15.
Su LK; Kohlmann W; Ward PA; Lynch PM
Hum Genet; 2002 Jul; 111(1):88-95. PubMed ID: 12136240
[TBL] [Abstract][Full Text] [Related]
16. [Detection of adenomatous polyposis coli gene mutations in 31 familial adenomatous polyposis families by using denaturing high performance liquid chromatography].
Cai SR; Zhang SZ; Zheng S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr; 25(2):164-7. PubMed ID: 18393237
[TBL] [Abstract][Full Text] [Related]
17. Transcript dosage effect in familial adenomatous polyposis: model offered by two kindreds with exon 9 APC gene mutations.
Curia MC; Esposito DL; Aceto G; Palmirotta R; Crognale S; Valanzano R; Ficari F; Tonelli F; Battista P; Mariani-Costantini R; Cama A
Hum Mutat; 1998; 11(3):197-201. PubMed ID: 9521420
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Familial adenomatous polyposis coli in the Czech population. I. Detection of an additional 3 mutations out of a total of 7 in exon 15 of the APC gene].
Jirásek V; Olschwang S; Boisson C; Janda J; Thomas G; Martásek P
Cas Lek Cesk; 1997 Dec; 136(23):733-8. PubMed ID: 9476377
[TBL] [Abstract][Full Text] [Related]
20. Maternal mosaicism for a second mutational event--a novel deletion--in a familial adenomatous polyposis family harboring a new germ-line mutation in the alternatively spliced-exon 9 region of APC.
Davidson S; Leshanski L; Rennert G; Eidelman S; Amikam D
Hum Mutat; 2002 Jan; 19(1):83-4. PubMed ID: 11754114
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
