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Role of congenital hypertrophy of the retinal pigment epithelium in the predictive diagnosis of familial adenomatous polyposis

✍ Scribed by D. G. Morton; J. Gibson; F. Macdonald; R. Brown; J. Haydon; R. Cullen; M. Rindl; M. Hulten; J. P. Neoptolemos; M. R. B. Keighley; C. M. McKeown

Publisher: John Wiley and Sons
Year: 1992
Tongue: English
Weight: 575 KB
Volume: 79
Category: Article
ISSN: 0007-1323
DOI: 10.1002/bjs.1800790733

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## Abstract Within 36 months of its formation the Northern Region Polyposis Registry had increased the number of identified gene carriers of familial adenomatous polyposis from 56 to 65 in a population of 3·1 million and had achieved a 15-fold increase in the number of at-risk relatives being regul