Genetic heterogeneity of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in families with familial adenomatous polyposis.-Reference-Cited by-同舟云学术

Genetic heterogeneity of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in families with familial adenomatous polyposis.

Published:1994-01-01 Issue:1 Volume:31 Page:55-58
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Hodgson S V,Bishop D T,Jay B

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference14 articles.

1. Hypertrophy of the retinal pigment epithelium associated with Gardner's syndrome;Blair, N.P.; Trempe, C.L.;Am J Ophthalmol,1980

2. Congenital hypertrophy of retinal pigment epithelium: a sign of familial adenomatous polyposis;Chapman, P.D.; Church, W.; Burn, J.; Gunn, A.;BMJ,1989

3. The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations;Burn, J.; Chapman, P.; Delhanty, J.;Jf Med Genet,1991

4. Histopathological features of congenital fundus lesions in familial adenomatous polyposis;Parker, J.A.; Kalnins, VI, Deck; J.H.N.;Can J Ophthalmol,1990

5. A clinicopathologic study of the eyes in familial adenomatous polyposis with extracolonic manifestations (Gardner's syndrome);Traboulsi, E.I.; Murphy, S.F.; de la Cruz, Z.C.; Maumenee, I.H.; Green, W.R.;Am J Ophthalmol,1990

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