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.
5. 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 01; 14 ( Pt 1)():18-22. PubMed ID: 10755094 [Abstract] [Full Text] [Related]
10. 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 Apr 01; 11 ( Pt 3)():298-300. PubMed ID: 9373466 [Abstract] [Full Text] [Related]
13. Congenital hypertrophy of retinal pigment epithelium (CHRPE) as a marker for familial adenomatous polyposis (FAP). Bertario L, Bandello F, Rossetti C, Sala P, Fortini E, Spinelli P, Gennari L, Pietroiusti M, Presciuttini S. Eur J Cancer Prev; 1993 Jan 01; 2(1):69-75. PubMed ID: 8381318 [Abstract] [Full Text] [Related]
16. [When is congenital hypertrophy of the retinal pigment epithelium (CHRPE) associated with the Gardner's syndrome? An overview with clinical examples]. Meyer CH, Becker R, Schmidt JC, Kroll P. Klin Monbl Augenheilkd; 2002 Sep 01; 219(9):644-8. PubMed ID: 12410463 [Abstract] [Full Text] [Related]
17. [Contribution of the ophthalmologist to presymptomatic diagnosis of familial adenomatous polyposis (FAP)]. Sommer E, Hinkel GK, Friedl W. Ophthalmologe; 1995 Dec 01; 92(6):809-16. PubMed ID: 8563429 [Abstract] [Full Text] [Related]