Citations for

1	APC, CHRPE
	A novel deletion at codon 441 of the APC gene associated with ophthalmic lesions (CHRPE) in a South African family.
	Grobbelaar JJ, et al.
	J Med Genet 33 : 384-386. 1996
2	APC, CHRPE, FAP
	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 78(11):2400-10.PMID: 8941012 [PubMed - indexed for MEDLINE] 1996
3	APC, CHRPE, FAP
	Severe Gardner syndrome in families with mutations restricted to a specific region of the APC gene.
	Davies DR, et al.
	Am J Hum Genet 57 : 1151-1158. 1995
4	CHRPE
	Genetic heterogeneity of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in families with familial adenomatous polyposis.
	Hodgson SV, et al.
	J Med Genet 31 : 55-58. 1994
5	CHRPE, APC, FAP
	Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients.
	Olschwang S, et al.
	Cell 75 : 959-968. 1993
6	APC, CHRPE, FAP
	A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epithelium.
	Lyons LA, et al.
	Am J Hum Genet 42 : 290-296. 1988